{{Rsnum
|rsid=56199535
|Gene=ABCC2
|Chromosome=10
|position=99818820
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ABCC2
}}{{omim
|id=601107
|rsnum=56199535
|variant=0001
}}

{{ClinVar
|rsid=56199535
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=101578577
|CHROM=10
|GMAF=0.0005
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050360000000040516110100
|GENEINFO=ABCC2:1244
|GENE_NAME=ABCC2
|GENE_ID=1244
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000010.10:g.101578577C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601107.0001
|CLNSIG=5
|CLNCUI=C0022350
|CLNDBN=Dubin-Johnson syndrome
|Disease=Dubin-Johnson syndrome
|CLNACC=RCV000008923.1
|Tags=PM;S3D;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0022350:237500:234:44553005
|COMMON=0
}}

{{on chip | FTDNA2}}
{{on chip | FTDNA}}