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rs776848753

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776848753(C;C)
Make rs776848753(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51935629
GeneATP7B
is asnp
is mentioned by
dbSNPrs776848753
ebirs776848753
HLIrs776848753
Exacrs776848753
Varsomers776848753
Maprs776848753
PheGenIrs776848753
hapmaprs776848753
1000 genomesrs776848753
hgdprs776848753
ensemblrs776848753
gopubmedrs776848753
geneviewrs776848753
scholarrs776848753
googlers776848753
pharmgkbrs776848753
gwascentralrs776848753
openSNPrs776848753
23andMers776848753
23andMe allrs776848753
SNP Nexus

SNPshotrs776848753
SNPdbers776848753
MSV3drs776848753
GWAS Ctlgrs776848753
Max Magnitude0
ClinVar
Risk rs776848753(A,C;A,C)
Alt rs776848753(A,C;A,C)
Reference rs776848753(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52509765G>A
CLNSRC
CLNACC RCV000169268.1,