{{Rsnum
|rsid = 11568372
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=2
|position=168990819
|Gene=ABCB11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ABCB11
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2
|id=603201
|rsnum=11568372
|variant=0002
}}

{{ClinVar
|rsid=11568372
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=169847329
|CHROM=2
|dbSNPBuildID=127
|SSR=16
|SAO=1
|VP=0x050370000000000503110100
|GENEINFO=ABCB11:8647
|GENE_NAME=ABCB11
|GENE_ID=8647
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.169847329T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603201.0002
|CLNSIG=5
|CLNCUI=C1866138
|CLNDBN=Progressive familial intrahepatic cholestasis 2; Cholestasis, benign recurrent intrahepatic 2
|Disease=Progressive familial intrahepatic cholestasis 2; Cholestasis
|CLNACC=RCV000006968.1; RCV000006969.1
|Tags=RV;PM;TPA;S3D;SLO;HD;GNO;OTHERKG;PH3;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1297:C1866138:601847:172:79304
}}

{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}