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rs17431184

From SNPedia

Orientationplus
Stabilizedplus
Make rs17431184(C;C)
Make rs17431184(C;T)
Make rs17431184(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position87960494
GenePTEN
is asnp
is mentioned by
dbSNPrs17431184
ebirs17431184
HLIrs17431184
Exacrs17431184
Varsomers17431184
Maprs17431184
PheGenIrs17431184
hapmaprs17431184
1000 genomesrs17431184
hgdprs17431184
ensemblrs17431184
gopubmedrs17431184
geneviewrs17431184
scholarrs17431184
googlers17431184
pharmgkbrs17431184
gwascentralrs17431184
openSNPrs17431184
23andMers17431184
23andMe allrs17431184
SNP Nexus

SNPshotrs17431184
SNPdbers17431184
MSV3drs17431184
GWAS Ctlgrs17431184
GMAF0.1478
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23068025] Association of PTEN genetic polymorphisms with atherosclerotic cerebral infarction in the Han Chinese 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 26541596] Association of genetic polymorphisms in PTEN and additional gene-gene interaction with risk of esophageal squamous cell carcinoma in Chinese Han population