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rs1064796067

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TCGAT;TCGAT) 0 common in clinvar
Chromosome10
Position87960991
GenePTEN
is asnp
is mentioned by
dbSNPrs1064796067
dbSNP (old)rs1064796067
ClinGenrs1064796067
ebirs1064796067
HLIrs1064796067
Exacrs1064796067
Gnomadrs1064796067
Varsomers1064796067
Maprs1064796067
PheGenIrs1064796067
Biobankrs1064796067
1000 genomesrs1064796067
hgdprs1064796067
ensemblrs1064796067
gopubmedrs1064796067
geneviewrs1064796067
scholarrs1064796067
googlers1064796067
pharmgkbrs1064796067
gwascentralrs1064796067
openSNPrs1064796067
23andMers1064796067
23andMe allrs1064796067
SNPshotrs1064796067
SNPdbers1064796067
MSV3drs1064796067
GWAS Ctlgrs1064796067
Max Magnitude0
ClinVar
Risk rs1064796067(-;-)
Alt rs1064796067(-;-)
Reference Rs1064796067(TCGAT;TCGAT)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89720748_89720752delTCGAT
CLNSRC
CLNACC RCV000483214.1,