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rs1064796054

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome13
Position51946443
GeneATP7B
is asnp
is mentioned by
dbSNPrs1064796054
dbSNP (old)rs1064796054
ClinGenrs1064796054
ebirs1064796054
HLIrs1064796054
Exacrs1064796054
Gnomadrs1064796054
Varsomers1064796054
Maprs1064796054
PheGenIrs1064796054
Biobankrs1064796054
1000 genomesrs1064796054
hgdprs1064796054
ensemblrs1064796054
gopubmedrs1064796054
geneviewrs1064796054
scholarrs1064796054
googlers1064796054
pharmgkbrs1064796054
gwascentralrs1064796054
openSNPrs1064796054
23andMers1064796054
23andMe allrs1064796054
SNPshotrs1064796054
SNPdbers1064796054
MSV3drs1064796054
GWAS Ctlgrs1064796054
Max Magnitude0
ClinVar
Risk rs1064796054(-;-)
Alt rs1064796054(-;-)
Reference Rs1064796054(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP7B
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.52520579delG
CLNSRC
CLNACC RCV000479903.1,