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rs587783307

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783307(A;C)
Make rs587783307(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51946333
GeneATP7B
is asnp
is mentioned by
dbSNPrs587783307
ebirs587783307
HLIrs587783307
Exacrs587783307
Varsomers587783307
Maprs587783307
PheGenIrs587783307
hapmaprs587783307
1000 genomesrs587783307
hgdprs587783307
ensemblrs587783307
gopubmedrs587783307
geneviewrs587783307
scholarrs587783307
googlers587783307
pharmgkbrs587783307
gwascentralrs587783307
openSNPrs587783307
23andMers587783307
23andMe allrs587783307
SNP Nexus

SNPshotrs587783307
SNPdbers587783307
MSV3drs587783307
GWAS Ctlgrs587783307
Max Magnitude0
ClinVar
Risk rs587783307(C;C)
Alt rs587783307(C;C)
Reference rs587783307(A;A)
Significance Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52520469T>G
CLNSRC
CLNACC RCV000145267.1,