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rs121908935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908935(C;C)
Make rs121908935(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position168976590
GeneABCB11
is asnp
is mentioned by
dbSNPrs121908935
ebirs121908935
HLIrs121908935
Exacrs121908935
Varsomers121908935
Maprs121908935
PheGenIrs121908935
hapmaprs121908935
1000 genomesrs121908935
hgdprs121908935
ensemblrs121908935
gopubmedrs121908935
geneviewrs121908935
scholarrs121908935
googlers121908935
pharmgkbrs121908935
gwascentralrs121908935
openSNPrs121908935
23andMers121908935
23andMe allrs121908935
SNP Nexus

SNPshotrs121908935
SNPdbers121908935
MSV3drs121908935
GWAS Ctlgrs121908935
Max Magnitude0
OMIM603201
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908935(C;C)
Alt rs121908935(C;C)
Reference rs121908935(G;G)
Significance Pathogenic
Disease Benign recurrent intrahepatic cholestasis 2
Variation info
Gene ABCB11
CLNDBN Benign recurrent intrahepatic cholestasis 2
Reversed 1
HGVS NC_000002.11:g.169833100C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006974.2,