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rs587783318

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783318(A;A)
Make rs587783318(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51935678
GeneATP7B
is asnp
is mentioned by
dbSNPrs587783318
ebirs587783318
HLIrs587783318
Exacrs587783318
Varsomers587783318
Maprs587783318
PheGenIrs587783318
hapmaprs587783318
1000 genomesrs587783318
hgdprs587783318
ensemblrs587783318
gopubmedrs587783318
geneviewrs587783318
scholarrs587783318
googlers587783318
pharmgkbrs587783318
gwascentralrs587783318
openSNPrs587783318
23andMers587783318
23andMe allrs587783318
SNP Nexus

SNPshotrs587783318
SNPdbers587783318
MSV3drs587783318
GWAS Ctlgrs587783318
Max Magnitude0
ClinVar
Risk rs587783318(A;A)
Alt rs587783318(A;A)
Reference rs587783318(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52509814C>T
CLNSRC
CLNACC RCV000145281.1,