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rs184868522

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs184868522(A;G)
Make rs184868522(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position51975122
GeneATP7B
is asnp
is mentioned by
dbSNPrs184868522
ebirs184868522
HLIrs184868522
Exacrs184868522
Varsomers184868522
Maprs184868522
PheGenIrs184868522
hapmaprs184868522
1000 genomesrs184868522
hgdprs184868522
ensemblrs184868522
gopubmedrs184868522
geneviewrs184868522
scholarrs184868522
googlers184868522
pharmgkbrs184868522
gwascentralrs184868522
openSNPrs184868522
23andMers184868522
23andMe allrs184868522
SNP Nexus

SNPshotrs184868522
SNPdbers184868522
MSV3drs184868522
GWAS Ctlgrs184868522
GMAF0.002296
Max Magnitude0
ClinVar
Risk rs184868522(G;G)
Alt rs184868522(G;G)
Reference rs184868522(A;A)
Significance Probable-Pathogenic
Disease Wilson's disease not provided
Variation info
Gene ATP7B
CLNDBN Wilson's disease not provided
Reversed 0
HGVS NC_000013.10:g.52549258A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029385.1, RCV000175512.1,