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rs1064793377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position25699254
GeneATP8A2
is asnp
is mentioned by
dbSNPrs1064793377
dbSNP (old)rs1064793377
ClinGenrs1064793377
ebirs1064793377
HLIrs1064793377
Exacrs1064793377
Gnomadrs1064793377
Varsomers1064793377
LitVarrs1064793377
Maprs1064793377
PheGenIrs1064793377
Biobankrs1064793377
1000 genomesrs1064793377
hgdprs1064793377
ensemblrs1064793377
gopubmedrs1064793377
geneviewrs1064793377
scholarrs1064793377
googlers1064793377
pharmgkbrs1064793377
gwascentralrs1064793377
openSNPrs1064793377
23andMers1064793377
23andMe allrs1064793377
SNPshotrs1064793377
SNPdbers1064793377
MSV3drs1064793377
GWAS Ctlgrs1064793377
Max Magnitude0
ClinVar
Risk rs1064793377(T;T)
Alt rs1064793377(T;T)
Reference Rs1064793377(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATP8A2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.26273392G>T
CLNSRC
CLNACC RCV000486844.1,