Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: HSD17B10 (Hsa) Molecular Consequence: synonymous variant
(GRCh38)X:53433743G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53433743G>A
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433743G>A
(GRCh38)X:53433812T>A
(Homo sapiens)Allele/Variant
Source: rs1373821788
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433812T>A
(GRCh38)X:53432250A>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432250A>T
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432250A>T
(GRCh38)X:53432328T>G
(Homo sapiens)Allele/Variant
Source: rs1569365820
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432328T>G
(GRCh38)X:53433770C>T
(Homo sapiens)Allele/Variant
Source: rs782158864
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433770C>T
(GRCh38)X:53431479T>C
(Homo sapiens)Allele/Variant
Source: rs1556894495
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431479T>C
(GRCh38)X:53434340T>C
(Homo sapiens)Allele/Variant
Source: rs897323903
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53434340T>C
(GRCh38)X:53434330G>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53434330G>T
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53434330G>T
(GRCh38)X:53432331A>G
(Homo sapiens)Allele/Variant
Source: rs782330394
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432331A>G
(GRCh38)X:53433725G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53433725G>A
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433725G>A
(GRCh38)X:53432361C>T
(Homo sapiens)Allele/Variant
Source: rs2146628349
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432361C>T
(GRCh38)X:53431524G>A
(Homo sapiens)Allele/Variant
Source: rs2075824833
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431524G>A
(GRCh38)X:53431994C>T
(Homo sapiens)Allele/Variant
Source: rs1161789651
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431994C>T
(GRCh38)X:53432024G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432024G>A
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432024G>A
(GRCh38)X:53432247A>G
(Homo sapiens)Allele/Variant
Source: rs1431860249
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432247A>G
(GRCh38)X:53432030C>G
(Homo sapiens)Allele/Variant
Source: rs781883925
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432030C>G
(GRCh38)X:53434340T>G
(Homo sapiens)Allele/Variant
Source: rs897323903
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53434340T>G
(GRCh38)X:53434334C>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53434334C>A
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53434334C>A
(GRCh38)X:53432286G>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432286G>T
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432286G>T
(GRCh38)X:53432325G>A
(Homo sapiens)Allele/Variant
Source: rs1556894661
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432325G>A
(GRCh38)X:53431440G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431440G>A
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431440G>A
(GRCh38)X:53433824A>C
(Homo sapiens)Allele/Variant
Source: rs782505983
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433824A>C
(GRCh38)X:53431819G>T
(Homo sapiens)Allele/Variant
Source: rs122462164
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431819G>T
(GRCh38)X:53431590C>G
(Homo sapiens)Allele/Variant
Source: rs1255652783
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431590C>G
(GRCh38)X:53431895A>C
(Homo sapiens)Allele/Variant
Source: rs2075826259
Genes: HSD17B10 (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)X:53431895A>C
(GRCh38)X:53433881C>T
(Homo sapiens)Allele/Variant
Source: rs1556894950
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433881C>T
(GRCh38)X:53432364T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432364T>G
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432364T>G
(GRCh38)X:53433734G>A
(Homo sapiens)Allele/Variant
Source: rs1569366312
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433734G>A
(GRCh38)X:53433773C>T
(Homo sapiens)Allele/Variant
Source: rs782719811
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433773C>T
(GRCh38)X:53432021G>A
(Homo sapiens)Allele/Variant
Source: rs182999706
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432021G>A
(GRCh38)X:53431482G>A
(Homo sapiens)Allele/Variant
Source: rs782783783
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431482G>A
(GRCh38)X:53431997G>A
(Homo sapiens)Allele/Variant
Source: rs2075826714
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431997G>A
(GRCh38)X:53433824A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53433824A>G
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433824A>G
(GRCh38)X:53432108G>A
(Homo sapiens)Allele/Variant
Source: rs797045616
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432108G>A
(GRCh38)X:53432297A>G
(Homo sapiens)Allele/Variant
Source: rs1416406199
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432297A>G
(GRCh38)X:53432301G>A
(Homo sapiens)Allele/Variant
Source: rs1395975082
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432301G>A
(GRCh38)X:53432409C>T
(Homo sapiens)Allele/Variant
Source: rs782466620
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432409C>T
(GRCh38)X:53431554T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431554T>C
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431554T>C
(GRCh38)X:53431850G>A
(Homo sapiens)Allele/Variant
Source: rs2075826144
Genes: HSD17B10 (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)X:53431850G>A
(GRCh38)X:53431862G>T
(Homo sapiens)Allele/Variant
Source: rs782388358
Genes: HSD17B10 (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)X:53431862G>T
(GRCh38)X:53431790A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431790A>G
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431790A>G
(GRCh38)X:53434331A>G
(Homo sapiens)Allele/Variant
Source: rs1556895056
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53434331A>G
(GRCh38)X:53432286G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432286G>A
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432286G>A
(GRCh38)X:53433767G>C
(Homo sapiens)Allele/Variant
Source: rs367982176
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433767G>C
(GRCh38)X:53431449A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431449A>G
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431449A>G
(GRCh38)X:53431467G>A
(Homo sapiens)Allele/Variant
Source: rs782119770
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431467G>A
(GRCh38)X:53432274G>C
(Homo sapiens)Allele/Variant
Source: rs1569365787
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432274G>C
(GRCh38)X:53432304C>T
(Homo sapiens)Allele/Variant
Source: rs1840417696
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432304C>T
(GRCh38)X:53433875C>G
(Homo sapiens)Allele/Variant
Source: rs1556894946
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433875C>G
(GRCh38)X:53432319C>T
(Homo sapiens)Allele/Variant
Source: rs1452727816
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432319C>T