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rs1085308045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome10
Position87933128
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308045
dbSNP (classic)rs1085308045
ClinGenrs1085308045
ebirs1085308045
HLIrs1085308045
Exacrs1085308045
Gnomadrs1085308045
Varsomers1085308045
LitVarrs1085308045
Maprs1085308045
PheGenIrs1085308045
Biobankrs1085308045
1000 genomesrs1085308045
hgdprs1085308045
ensemblrs1085308045
geneviewrs1085308045
scholarrs1085308045
googlers1085308045
pharmgkbrs1085308045
gwascentralrs1085308045
openSNPrs1085308045
23andMers1085308045
23andMe allrs1085308045
SNPshotrs1085308045
SNPdbers1085308045
MSV3drs1085308045
GWAS Ctlgrs1085308045
Max Magnitude0
ClinVar
Risk rs1085308045(G;G)
Alt rs1085308045(G;G)
Reference Rs1085308045(C;C)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89692885C>G
CLNSRC
CLNACC RCV000490619.1,