Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: HSD17B10 (Hsa)
(GRCh38)X:53431969C>T
(Homo sapiens)Allele/Variant
Source: rs1556894578
Genes: HSD17B10 (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)X:53431969C>T
(GRCh38)X:53434026G>A
(Homo sapiens)Allele/Variant
Source: rs139681190
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53434026G>A
(GRCh38)X:53434302G>C
(Homo sapiens)Allele/Variant
Source: rs911505039
Genes: HSD17B10 (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)X:53434302G>C
(GRCh38)X:53432321C>T
(Homo sapiens)Allele/Variant
Source: rs201378370
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432321C>T
(GRCh38)X:53431605T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431605T>C
Genes: HSD17B10 (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)X:53431605T>C
(GRCh38)X:53431801G>T
(Homo sapiens)Allele/Variant
Source: rs886037927
Genes: HSD17B10 (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)X:53431801G>T
(GRCh38)X:53433829G>C
(Homo sapiens)Allele/Variant
Source: rs1348504554
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433829G>C
(GRCh38)X:53433892A>G
(Homo sapiens)Allele/Variant
Source: rs1827330997
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433892A>G
(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:53433790G>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53433790G>C
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433790G>C
(GRCh38)X:53434333A>G
(Homo sapiens)Allele/Variant
Source: rs781935025
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53434333A>G
(GRCh38)X:53431484G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431484G>A
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431484G>A
(GRCh38)X:53431848A>C
(Homo sapiens)Allele/Variant
Source: rs2146627904
Genes: HSD17B10 (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)X:53431848A>C
(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:53431556T>C
(Homo sapiens)Allele/Variant
Source: rs886041974
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53431556T>C
(GRCh38)X:53431921G>T
(Homo sapiens)Allele/Variant
Source: rs1556894569
Genes: HSD17B10 (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)X:53431921G>T
(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: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:53432271C>G
(Homo sapiens)Allele/Variant
Source: rs2075827834
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432271C>G
(GRCh38)X:53432371G>C
(Homo sapiens)Allele/Variant
Source: rs781966115
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432371G>C
(GRCh38)X:53432381G>C
(Homo sapiens)Allele/Variant
Source: rs374438347
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432381G>C
(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:53431885C>T
(Homo sapiens)Allele/Variant
Source: rs2146627918
Genes: HSD17B10 (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)X:53431885C>T
(GRCh38)X:53432065C>T
(Homo sapiens)Allele/Variant
Source: rs2146628049
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432065C>T
(GRCh38)X:53432086G>A
(Homo sapiens)Allele/Variant
Source: rs28935475
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432086G>A
(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: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:53432094T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432094T>C
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432094T>C
(GRCh38)X:53432410A>G
(Homo sapiens)Allele/Variant
Source: rs104886492
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432410A>G
(GRCh38)X:53433771T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53433771T>G
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433771T>G
(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:53432110G>C
(Homo sapiens)Allele/Variant
Source: rs28935476
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432110G>C
(GRCh38)X:53433877C>T
(Homo sapiens)Allele/Variant
Source: rs782206781
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53433877C>T
(GRCh38)X:53431786G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431786G>A
Genes: HSD17B10 (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)X:53431786G>A
(GRCh38)X:53431924G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53431924G>A
Genes: HSD17B10 (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)X:53431924G>A
(GRCh38)X:53431613T>A
(Homo sapiens)Allele/Variant
Source: rs1556894522
Genes: HSD17B10 (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)X:53431613T>A
(GRCh38)X:53432290T>G
(Homo sapiens)Allele/Variant
Source: rs2075827990
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432290T>G
(GRCh38)X:53432311C>A
(Homo sapiens)Allele/Variant
Source: rs2075828065
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432311C>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:53432129T>C
(Homo sapiens)Allele/Variant
Source: rs782644415
Genes: HSD17B10 (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)X:53432129T>C
(GRCh38)X:53432411C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432411C>T
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432411C>T
(GRCh38)X:53431979C>T
(Homo sapiens)Allele/Variant
Source: rs190913381
Genes: HSD17B10 (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)X:53431979C>T
(GRCh38)X:53432073C>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53432073C>G
Genes: HSD17B10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:53432073C>G
(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:53434309A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.53434309A>G
Genes: HSD17B10 (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)X:53434309A>G