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rs1064796886

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome10
Position87894058
GenePTEN
is asnp
is mentioned by
dbSNPrs1064796886
dbSNP (classic)rs1064796886
ClinGenrs1064796886
ebirs1064796886
HLIrs1064796886
Exacrs1064796886
Gnomadrs1064796886
Varsomers1064796886
LitVarrs1064796886
Maprs1064796886
PheGenIrs1064796886
Biobankrs1064796886
1000 genomesrs1064796886
hgdprs1064796886
ensemblrs1064796886
geneviewrs1064796886
scholarrs1064796886
googlers1064796886
pharmgkbrs1064796886
gwascentralrs1064796886
openSNPrs1064796886
23andMers1064796886
23andMe allrs1064796886
SNPshotrs1064796886
SNPdbers1064796886
MSV3drs1064796886
GWAS Ctlgrs1064796886
Max Magnitude0
ClinVar
Risk rs1064796886(G;G)
Alt rs1064796886(G;G)
Reference Rs1064796886(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89653815C>G
CLNSRC
CLNACC RCV000484991.1,