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rs1085307612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome10
Position87961039
GenePTEN
is asnp
is mentioned by
dbSNPrs1085307612
dbSNP (classic)rs1085307612
ClinGenrs1085307612
ebirs1085307612
HLIrs1085307612
Exacrs1085307612
Gnomadrs1085307612
Varsomers1085307612
LitVarrs1085307612
Maprs1085307612
PheGenIrs1085307612
Biobankrs1085307612
1000 genomesrs1085307612
hgdprs1085307612
ensemblrs1085307612
geneviewrs1085307612
scholarrs1085307612
googlers1085307612
pharmgkbrs1085307612
gwascentralrs1085307612
openSNPrs1085307612
23andMers1085307612
23andMe allrs1085307612
SNPshotrs1085307612
SNPdbers1085307612
MSV3drs1085307612
GWAS Ctlgrs1085307612
Max Magnitude0
ClinVar
Risk rs1085307612(-;-)
Alt rs1085307612(-;-)
Reference Rs1085307612(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89720796delT
CLNSRC
CLNACC RCV000489822.1,