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rs1064796648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position78031425
GeneATP7A
is asnp
is mentioned by
dbSNPrs1064796648
dbSNP (old)rs1064796648
ClinGenrs1064796648
ebirs1064796648
HLIrs1064796648
Exacrs1064796648
Gnomadrs1064796648
Varsomers1064796648
LitVarrs1064796648
Maprs1064796648
PheGenIrs1064796648
Biobankrs1064796648
1000 genomesrs1064796648
hgdprs1064796648
ensemblrs1064796648
gopubmedrs1064796648
geneviewrs1064796648
scholarrs1064796648
googlers1064796648
pharmgkbrs1064796648
gwascentralrs1064796648
openSNPrs1064796648
23andMers1064796648
23andMe allrs1064796648
SNPshotrs1064796648
SNPdbers1064796648
MSV3drs1064796648
GWAS Ctlgrs1064796648
Max Magnitude0
ClinVar
Risk rs1064796648(T;T)
Alt rs1064796648(T;T)
Reference Rs1064796648(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP7A
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.77286923C>T
CLNSRC
CLNACC RCV000484292.1,