{{Rsnum
|rsid=121917848
|Chromosome=13
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC10A2
|position=103051290
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC10A2
}}{{omim
|id=601295
|rsnum=121917848
|variant=0001
}}{{ClinVar
|rsid=121917848
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=103703640
|CHROM=13
|dbSNPBuildID=137
|SSR=0
|SAO=0
|VP=0x050060000000000002110100
|GENEINFO=SLC10A2:6555
|GENE_NAME=SLC10A2
|GENE_ID=6555
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.103703640A>G
|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;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2750087:613291
}}