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rs587783317

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783317(A;A)
Make rs587783317(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51937276
GeneATP7B
is asnp
is mentioned by
dbSNPrs587783317
ebirs587783317
HLIrs587783317
Exacrs587783317
Varsomers587783317
Maprs587783317
PheGenIrs587783317
hapmaprs587783317
1000 genomesrs587783317
hgdprs587783317
ensemblrs587783317
gopubmedrs587783317
geneviewrs587783317
scholarrs587783317
googlers587783317
pharmgkbrs587783317
gwascentralrs587783317
openSNPrs587783317
23andMers587783317
23andMe allrs587783317
SNP Nexus

SNPshotrs587783317
SNPdbers587783317
MSV3drs587783317
GWAS Ctlgrs587783317
Max Magnitude0
ClinVar
Risk rs587783317(A;A)
Alt rs587783317(A;A)
Reference rs587783317(G;G)
Significance Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52511412C>T
CLNSRC
CLNACC RCV000145280.1,