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rs34937870

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs34937870(A;A)
Make rs34937870(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position99842094
GeneABCC2
is asnp
is mentioned by
dbSNPrs34937870
ebirs34937870
HLIrs34937870
Exacrs34937870
Varsomers34937870
Maprs34937870
PheGenIrs34937870
hapmaprs34937870
1000 genomesrs34937870
hgdprs34937870
ensemblrs34937870
gopubmedrs34937870
geneviewrs34937870
scholarrs34937870
googlers34937870
pharmgkbrs34937870
gwascentralrs34937870
openSNPrs34937870
23andMers34937870
23andMe allrs34937870
SNP Nexus

SNPshotrs34937870
SNPdbers34937870
MSV3drs34937870
GWAS Ctlgrs34937870
Max Magnitude0
ClinVar
Risk rs34937870(A,T;A,T)
Alt rs34937870(A,T;A,T)
Reference rs34937870(G;G)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101601851G>A
CLNSRC
CLNACC RCV000190561.1,