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rs372436901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs372436901(G;G)
Make rs372436901(G;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position51960300
GeneATP7B
is asnp
is mentioned by
dbSNPrs372436901
ebirs372436901
HLIrs372436901
Exacrs372436901
Varsomers372436901
Maprs372436901
PheGenIrs372436901
hapmaprs372436901
1000 genomesrs372436901
hgdprs372436901
ensemblrs372436901
gopubmedrs372436901
geneviewrs372436901
scholarrs372436901
googlers372436901
pharmgkbrs372436901
gwascentralrs372436901
openSNPrs372436901
23andMers372436901
23andMe allrs372436901
SNP Nexus

SNPshotrs372436901
SNPdbers372436901
MSV3drs372436901
GWAS Ctlgrs372436901
Max Magnitude0
ClinVar
Risk rs372436901(C,G;C,G)
Alt rs372436901(C,G;C,G)
Reference rs372436901(T;T)
Significance Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52534436T>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000145255.1,