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rs863224848

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224848(C;G)
Make rs863224848(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position51946394
GeneATP7B
is asnp
is mentioned by
dbSNPrs863224848
ebirs863224848
HLIrs863224848
Exacrs863224848
Varsomers863224848
Maprs863224848
PheGenIrs863224848
hapmaprs863224848
1000 genomesrs863224848
hgdprs863224848
ensemblrs863224848
gopubmedrs863224848
geneviewrs863224848
scholarrs863224848
googlers863224848
pharmgkbrs863224848
gwascentralrs863224848
openSNPrs863224848
23andMers863224848
23andMe allrs863224848
SNP Nexus

SNPshotrs863224848
SNPdbers863224848
MSV3drs863224848
GWAS Ctlgrs863224848
Max Magnitude0
ClinVar
Risk rs863224848(G;G)
Alt rs863224848(G;G)
Reference rs863224848(C;C)
Significance Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52520530G>C
CLNSRC
CLNACC RCV000196058.1,