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rs367956522

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs367956522(C;C)
Make rs367956522(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51949798
GeneATP7B
is asnp
is mentioned by
dbSNPrs367956522
ebirs367956522
HLIrs367956522
Exacrs367956522
Varsomers367956522
Maprs367956522
PheGenIrs367956522
hapmaprs367956522
1000 genomesrs367956522
hgdprs367956522
ensemblrs367956522
gopubmedrs367956522
geneviewrs367956522
scholarrs367956522
googlers367956522
pharmgkbrs367956522
gwascentralrs367956522
openSNPrs367956522
23andMers367956522
23andMe allrs367956522
SNP Nexus

SNPshotrs367956522
SNPdbers367956522
MSV3drs367956522
GWAS Ctlgrs367956522
Max Magnitude0
ClinVar
Risk rs367956522(C;C)
Alt rs367956522(C;C)
Reference rs367956522(T;T)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52523934T>C
CLNSRC
CLNACC RCV000169025.1,