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rs1064797072

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position51944116
GeneATP7B
is asnp
is mentioned by
dbSNPrs1064797072
dbSNP (classic)rs1064797072
ClinGenrs1064797072
ebirs1064797072
HLIrs1064797072
Exacrs1064797072
Gnomadrs1064797072
Varsomers1064797072
LitVarrs1064797072
Maprs1064797072
PheGenIrs1064797072
Biobankrs1064797072
1000 genomesrs1064797072
hgdprs1064797072
ensemblrs1064797072
geneviewrs1064797072
scholarrs1064797072
googlers1064797072
pharmgkbrs1064797072
gwascentralrs1064797072
openSNPrs1064797072
23andMers1064797072
23andMe allrs1064797072
SNPshotrs1064797072
SNPdbers1064797072
MSV3drs1064797072
GWAS Ctlgrs1064797072
Max Magnitude0
ClinVar
Risk rs1064797072(T;T)
Alt rs1064797072(T;T)
Reference Rs1064797072(G;G)
Significance Pathogenic
Disease Wilson disease
Variation info
Gene ATP7B
CLNDBN Wilson disease
Reversed 1
HGVS NC_000013.10:g.52518252C>A
CLNSRC
CLNACC RCV000487452.1,