{{Rsnum
|rsid=387906390
|Chromosome=13
|Orientation=minus
|geno1=(AAG;AAG)
|geno2=(AAG;CTT)
|geno3=(CTT;CTT)
|Gene=SLC10A2
|position=103052619
|Gene_s=SLC10A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=AAAG
|CHROM=13
|CLNACC=RCV000008725.1
|CLNALLE=1
|CLNDBN=Bile acid malabsorption, primary
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2750087:613291
|CLNHGVS=NC_000013.10:g.103704969_103704971delCTTinsAAG
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601295.0002
|Disease=Bile acid malabsorption
|FwdALT=CTT
|FwdREF=AAG
|REF=ACTT
|RSPOS=103704968
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=MNV
|VP=0x050060000000000002110800
|WGT=0
|dbSNPBuildID=137
|rsid=387906390
|GENEINFO=SLC10A2:6555
|GENE_ID=6555
|GENE_NAME=SLC10A2
}}