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rs8187797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome7
Position87439814
GeneABCB4
is asnp
is mentioned by
dbSNPrs8187797
ebirs8187797
HLIrs8187797
Exacrs8187797
Varsomers8187797
Maprs8187797
PheGenIrs8187797
hapmaprs8187797
1000 genomesrs8187797
hgdprs8187797
ensemblrs8187797
gopubmedrs8187797
geneviewrs8187797
scholarrs8187797
googlers8187797
pharmgkbrs8187797
gwascentralrs8187797
openSNPrs8187797
23andMers8187797
23andMe allrs8187797
SNP Nexus

SNPshotrs8187797
SNPdbers8187797
MSV3drs8187797
GWAS Ctlgrs8187797
Max Magnitude0

[PMID 25802476OA-icon.png] The Affymetrix DMET Plus Platform Reveals Unique Distribution of ADME-Related Variants in Ethnic Arabs


ClinVar
Risk rs8187797(G;G)
Alt rs8187797(G;G)
Reference rs8187797(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ABCB4
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.87069130C>G
CLNSRC
CLNACC RCV000174682.1,