rs2299939

Orientation

plus

Stabilized

plus

Make rs2299939(A;A)

Make rs2299939(A;C)

Make rs2299939(C;C)

Reference

GRCh38 38.1/142

Chromosome

10

Position

87897393

Gene

PTEN

is a	snp
is	mentioned by
dbSNP	rs2299939
dbSNP (classic)	rs2299939
ClinGen	rs2299939
ebi	rs2299939
HLI	rs2299939
Exac	rs2299939
Gnomad	rs2299939
Varsome	rs2299939
LitVar	rs2299939
Map	rs2299939
PheGenI	rs2299939
Biobank	rs2299939
1000 genomes	rs2299939
hgdp	rs2299939
ensembl	rs2299939
geneview	rs2299939
scholar	rs2299939
google	rs2299939
pharmgkb	rs2299939
gwascentral	rs2299939
openSNP	rs2299939
23andMe	rs2299939
SNPshot	rs2299939
SNPdbe	rs2299939
MSV3d	rs2299939
GWAS Ctlg	rs2299939

GMAF

0.1474

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

[PMID 23068025] Association of PTEN genetic polymorphisms with atherosclerotic cerebral infarction in the Han Chinese population

[PMID 16331670] Association of the phosphatase and tensin homolog gene (PTEN) with smoking initiation and nicotine dependence.

[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.

[PMID 19164214] Genetic variations in the PI3K/PTEN/AKT/mTOR pathway are associated with clinical outcomes in esophageal cancer patients treated with chemoradiotherapy.

[PMID 19673018] No association between phosphatase and tensin homolog genetic polymorphisms and colon cancer.

[PMID 26541596] Association of genetic polymorphisms in PTEN and additional gene-gene interaction with risk of esophageal squamous cell carcinoma in Chinese Han population