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rs1085308051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome10
Position87933229
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308051
dbSNP (old)rs1085308051
ClinGenrs1085308051
ebirs1085308051
HLIrs1085308051
Exacrs1085308051
Gnomadrs1085308051
Varsomers1085308051
Maprs1085308051
PheGenIrs1085308051
Biobankrs1085308051
1000 genomesrs1085308051
hgdprs1085308051
ensemblrs1085308051
gopubmedrs1085308051
geneviewrs1085308051
scholarrs1085308051
googlers1085308051
pharmgkbrs1085308051
gwascentralrs1085308051
openSNPrs1085308051
23andMers1085308051
23andMe allrs1085308051
SNPshotrs1085308051
SNPdbers1085308051
MSV3drs1085308051
GWAS Ctlgrs1085308051
Max Magnitude0
ClinVar
Risk rs1085308051(G;G)
Alt rs1085308051(G;G)
Reference Rs1085308051(A;A)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692986A>G
CLNSRC
CLNACC RCV000490604.1,