{{Rsnum
|rsid=72547505
|Gene=SLC10A2
|Chromosome=13
|position=103049423
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SLC10A2
}}{{omim
|id=601295
|rsnum=72547505
|variant=0001
}}

{{ClinVar
|rsid=72547505
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=103701773
|CHROM=13
|GMAF=0.0009
|dbSNPBuildID=130
|SSR=0
|SAO=0
|VP=0x050068000000040016110100
|GENEINFO=SLC10A2:6555
|GENE_NAME=SLC10A2
|GENE_ID=6555
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.103701773G>A
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601295.0001
|CLNSIG=5
|CLNCUI=C2750087; C2750087
|CLNDBN=Bile acid malabsorption, primary
|Disease=Bile acid malabsorption
|CLNACC=RCV000008724.2
|Tags=RV;PM;PMC;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183; .
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2750087:613291
|COMMON=0
}}

{{PMID|19823678|OA=1
}} A variant of the SLC10A2 gene encoding the apical sodium-dependent bile acid transporter is a risk factor for gallstone disease.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}