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rs749472361

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs749472361(A;A)
Make rs749472361(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position51937484
GeneATP7B
is asnp
is mentioned by
dbSNPrs749472361
ebirs749472361
HLIrs749472361
Exacrs749472361
Varsomers749472361
Maprs749472361
PheGenIrs749472361
hapmaprs749472361
1000 genomesrs749472361
hgdprs749472361
ensemblrs749472361
gopubmedrs749472361
geneviewrs749472361
scholarrs749472361
googlers749472361
pharmgkbrs749472361
gwascentralrs749472361
openSNPrs749472361
23andMers749472361
23andMe allrs749472361
SNP Nexus

SNPshotrs749472361
SNPdbers749472361
MSV3drs749472361
GWAS Ctlgrs749472361
Max Magnitude0
ClinVar
Risk rs749472361(A;A)
Alt rs749472361(A;A)
Reference rs749472361(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 0
HGVS NC_000013.10:g.52511620G>A
CLNSRC
CLNACC RCV000169572.1,