Version: 8.2.0Date: Wed Aug 27 2025
Category
LRP4-AS1
(Homo sapiens)Gene
Name: LRP4 antisense RNA 1
Synonyms: RP11-411D10.1
Source: HGNC:44128
Biotype: ncRNA gene
Symbol: LRP4-AS1 (Hsa)
Symbol: LRP4-AS1
(GRCh38)11:46873399G>C
(Homo sapiens)Allele/Variant
Source: rs1314468807
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46873399G>C
(GRCh38)11:46873415G>A
(Homo sapiens)Allele/Variant
Source: rs372569948
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46873415G>A
(GRCh38)11:46862708G>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.46862708G>T
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46862708G>T
(GRCh38)11:46862672T>C
(Homo sapiens)Allele/Variant
Source: rs765647853
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46862672T>C
(GRCh38)11:46862744G>A
(Homo sapiens)Allele/Variant
Source: rs138596351
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46862744G>A
(GRCh38)11:46856731C>T
(Homo sapiens)Allele/Variant
Source: rs188545674
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46856731C>T
(GRCh38)11:46856903A>G
(Homo sapiens)Allele/Variant
Source: rs76159791
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46856903A>G
(GRCh38)11:46858604G>A
(Homo sapiens)Allele/Variant
Source: rs561326679
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46858604G>A
(GRCh38)11:46858929C>T
(Homo sapiens)Allele/Variant
Source: rs147627264
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46858929C>T
(GRCh38)11:46859196G>C
(Homo sapiens)Allele/Variant
Source: rs560166088
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859196G>C
(GRCh38)11:46873595T>A
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.46873595T>A
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46873595T>A
(GRCh38)11:46858203G>A
(Homo sapiens)Allele/Variant
Source: rs886048344
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46858203G>A
(GRCh38)11:46858678G>A
(Homo sapiens)Allele/Variant
Source: rs886048347
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46858678G>A
(GRCh38)11:46864493C>T
(Homo sapiens)Allele/Variant
Source: rs2134765445
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46864493C>T
(GRCh38)11:46868107G>C
(Homo sapiens)Allele/Variant
Source: rs2134775125
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46868107G>C
(GRCh38)11:46868642A>G
(Homo sapiens)Allele/Variant
Source: rs2134776522
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46868642A>G
(GRCh38)11:46869097G>A
(Homo sapiens)Allele/Variant
Source: rs200270681
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46869097G>A
(GRCh38)11:46862616T>C
(Homo sapiens)Allele/Variant
Source: rs758146599
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46862616T>C
(GRCh38)11:46873559C>G
(Homo sapiens)Allele/Variant
Source: rs2134789849
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46873559C>G
(GRCh38)11:46873172G>A
(Homo sapiens)Allele/Variant
Source: rs1565780905
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46873172G>A
(GRCh38)11:46867965T>C
(Homo sapiens)Allele/Variant
Source: rs376251083
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46867965T>C
(GRCh38)11:46868876T>G
(Homo sapiens)Allele/Variant
Source: rs112479534
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46868876T>G
(GRCh38)11:46862753G>A
(Homo sapiens)Allele/Variant
Source: rs775832104
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46862753G>A
(GRCh38)11:46862896C>T
(Homo sapiens)Allele/Variant
Source: rs72897626
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46862896C>T
(GRCh38)11:46873605C>T
(Homo sapiens)Allele/Variant
Source: rs773322174
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46873605C>T
(GRCh38)11:46873755T>C
(Homo sapiens)Allele/Variant
Source: rs7111229
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46873755T>C
(GRCh38)11:46857437G>A
(Homo sapiens)Allele/Variant
Source: rs1420065241
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46857437G>A
(GRCh38)11:46859029G>A
(Homo sapiens)Allele/Variant
Source: rs372637156
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859029G>A
(GRCh38)11:46859047C>T
(Homo sapiens)Allele/Variant
Source: rs779079160
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859047C>T
(GRCh38)11:46859145G>A
(Homo sapiens)Allele/Variant
Source: rs200514161
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859145G>A
(GRCh38)11:46857516G>A
(Homo sapiens)Allele/Variant
Source: rs1940410910
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46857516G>A
(GRCh38)11:46857710C>G
(Homo sapiens)Allele/Variant
Source: rs1259687722
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46857710C>G
(GRCh38)11:46858722G>T
(Homo sapiens)Allele/Variant
Source: rs77376145
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46858722G>T
(GRCh38)11:46859116G>A
(Homo sapiens)Allele/Variant
Source: rs368840169
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859116G>A
(GRCh38)11:46859127A>G
(Homo sapiens)Allele/Variant
Source: rs767372541
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859127A>G
(GRCh38)11:46859160C>A
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.46859160C>A
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859160C>A
(GRCh38)11:46859169C>T
(Homo sapiens)Allele/Variant
Source: rs149687723
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859169C>T
(GRCh38)11:46859177A>G
(Homo sapiens)Allele/Variant
Source: rs769426991
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859177A>G
(GRCh38)11:46859181A>G
(Homo sapiens)Allele/Variant
Source: rs144350829
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859181A>G
(GRCh38)11:46859188C>A
(Homo sapiens)Allele/Variant
Source: rs770309253
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859188C>A
(GRCh38)11:46859201C>G
(Homo sapiens)Allele/Variant
Source: rs142462686
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46859201C>G
(GRCh38)11:46864457A>G
(Homo sapiens)Allele/Variant
Source: rs776705313
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46864457A>G
(GRCh38)11:46864513G>A
(Homo sapiens)Allele/Variant
Source: rs372105627
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46864513G>A
(GRCh38)11:46865134C>T
(Homo sapiens)Allele/Variant
Source: rs1002830453
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46865134C>T
(GRCh38)11:46865164G>A
(Homo sapiens)Allele/Variant
Source: rs1372975393
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46865164G>A
(GRCh38)11:46867996C>A
(Homo sapiens)Allele/Variant
Source: rs369034386
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46867996C>A
(GRCh38)11:46868006C>T
(Homo sapiens)Allele/Variant
Source: rs751407728
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46868006C>T
(GRCh38)11:46868628G>A
(Homo sapiens)Allele/Variant
Source: rs150734530
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46868628G>A
(GRCh38)11:46868652C>T
(Homo sapiens)Allele/Variant
Source: rs143849188
Genes: LRP4-AS1 (Hsa), LRP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:46868652C>T