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rs2673836

From SNPedia

Orientationplus
Stabilizedplus
Make rs2673836(A;A)
Make rs2673836(A;G)
Make rs2673836(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position87880205
GenePTEN
is asnp
is mentioned by
dbSNPrs2673836
ebirs2673836
HLIrs2673836
Exacrs2673836
Varsomers2673836
Maprs2673836
PheGenIrs2673836
hapmaprs2673836
1000 genomesrs2673836
hgdprs2673836
ensemblrs2673836
gopubmedrs2673836
geneviewrs2673836
scholarrs2673836
googlers2673836
pharmgkbrs2673836
gwascentralrs2673836
openSNPrs2673836
23andMers2673836
23andMe allrs2673836
SNP Nexus

SNPshotrs2673836
SNPdbers2673836
MSV3drs2673836
GWAS Ctlgrs2673836
GMAF0.1116
Max Magnitude

[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.