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rs701848

From SNPedia

Orientationplus
Stabilizedplus
Make rs701848(C;C)
Make rs701848(C;T)
Make rs701848(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position87966988
GenePTEN
is asnp
is mentioned by
dbSNPrs701848
ebirs701848
HLIrs701848
Exacrs701848
Varsomers701848
Maprs701848
PheGenIrs701848
hapmaprs701848
1000 genomesrs701848
hgdprs701848
ensemblrs701848
gopubmedrs701848
geneviewrs701848
scholarrs701848
googlers701848
pharmgkbrs701848
gwascentralrs701848
openSNPrs701848
23andMers701848
23andMe allrs701848
SNP Nexus

SNPshotrs701848
SNPdbers701848
MSV3drs701848
GWAS Ctlgrs701848
GMAF0.3416
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19625176OA-icon.png] PTEN identified as important risk factor of chronic obstructive pulmonary disease


[PMID 21138334] Association of PTEN Polymorphisms with Susceptibility to Hepatocellular Carcinoma in a Chinese Han Population


[PMID 17033968OA-icon.png] Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.


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


[PMID 19237173] Bcl2 -938C/A polymorphism carries increased risk of biochemical recurrence after radical prostatectomy.


[PMID 22336889] Association of genetic polymorphisms in MDM2, PTEN and P53 with risk of esophageal squamous cell carcinoma.


[PMID 23209702OA-icon.png] A Functional Variant in the MTOR Promoter Modulates Its Expression and Is Associated with Renal Cell Cancer Risk


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