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rs786204483

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204483(A;A)
Make rs786204483(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position51942497
GeneATP7B
is asnp
is mentioned by
dbSNPrs786204483
ebirs786204483
HLIrs786204483
Exacrs786204483
Varsomers786204483
Maprs786204483
PheGenIrs786204483
hapmaprs786204483
1000 genomesrs786204483
hgdprs786204483
ensemblrs786204483
gopubmedrs786204483
geneviewrs786204483
scholarrs786204483
googlers786204483
pharmgkbrs786204483
gwascentralrs786204483
openSNPrs786204483
23andMers786204483
23andMe allrs786204483
SNP Nexus

SNPshotrs786204483
SNPdbers786204483
MSV3drs786204483
GWAS Ctlgrs786204483
Max Magnitude0
ClinVar
Risk rs786204483(A;A)
Alt rs786204483(A;A)
Reference rs786204483(G;G)
Significance Probable-Pathogenic
Disease Wilson's disease
Variation info
Gene ATP7B
CLNDBN Wilson's disease
Reversed 1
HGVS NC_000013.10:g.52516633C>T
CLNSRC
CLNACC RCV000169142.1,