{{Rsnum
|rsid=104894518
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HSD3B7
|position=30986612
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HSD3B7
}}{{omim
|id=607764
|rsnum=104894518
|variant=0004
}}{{ClinVar
|rsid=104894518
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=30997933
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=HSD3B7:80270
|GENE_NAME=HSD3B7
|GENE_ID=80270
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.30997933G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607764.0004
|CLNSIG=5
|CLNCUI=C1843116
|CLNDBN=Bile acid synthesis defect, congenital, 1
|Disease=Bile acid synthesis defect
|CLNACC=RCV000003018.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1843116:607765:79301
}}