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rs587783306

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587783306(A;A)
Make rs587783306(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51949661
GeneATP7B
is asnp
is mentioned by
dbSNPrs587783306
ebirs587783306
HLIrs587783306
Exacrs587783306
Varsomers587783306
Maprs587783306
PheGenIrs587783306
hapmaprs587783306
1000 genomesrs587783306
hgdprs587783306
ensemblrs587783306
gopubmedrs587783306
geneviewrs587783306
scholarrs587783306
googlers587783306
pharmgkbrs587783306
gwascentralrs587783306
openSNPrs587783306
23andMers587783306
23andMe allrs587783306
SNP Nexus

SNPshotrs587783306
SNPdbers587783306
MSV3drs587783306
GWAS Ctlgrs587783306
Max Magnitude0
ClinVar
Risk rs587783306(A;A)
Alt rs587783306(A;A)
Reference Rs587783306(G;G)
Significance Pathogenic
Disease Wilson disease
Variation info
Gene ATP7B
CLNDBN Wilson disease
Reversed 1
HGVS NC_000013.10:g.52523797C>T
CLNSRC
CLNACC RCV000145266.1,