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rs1085308053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome10
Position87952230
GenePTEN
is asnp
is mentioned by
dbSNPrs1085308053
dbSNP (old)rs1085308053
ClinGenrs1085308053
ebirs1085308053
HLIrs1085308053
Exacrs1085308053
Gnomadrs1085308053
Varsomers1085308053
Maprs1085308053
PheGenIrs1085308053
Biobankrs1085308053
1000 genomesrs1085308053
hgdprs1085308053
ensemblrs1085308053
gopubmedrs1085308053
geneviewrs1085308053
scholarrs1085308053
googlers1085308053
pharmgkbrs1085308053
gwascentralrs1085308053
openSNPrs1085308053
23andMers1085308053
23andMe allrs1085308053
SNPshotrs1085308053
SNPdbers1085308053
MSV3drs1085308053
GWAS Ctlgrs1085308053
Max Magnitude0
ClinVar
Risk rs1085308053(T;T)
Alt rs1085308053(T;T)
Reference Rs1085308053(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.89711987C>T
CLNSRC
CLNACC RCV000490576.1,