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rs10490920

From SNPedia

Orientationplus
Stabilizedplus
Make rs10490920(C;C)
Make rs10490920(C;T)
Make rs10490920(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position87925886
GenePTEN
is asnp
is mentioned by
dbSNPrs10490920
dbSNP (classic)rs10490920
ClinGenrs10490920
ebirs10490920
HLIrs10490920
Exacrs10490920
Gnomadrs10490920
Varsomers10490920
LitVarrs10490920
Maprs10490920
PheGenIrs10490920
Biobankrs10490920
1000 genomesrs10490920
hgdprs10490920
ensemblrs10490920
geneviewrs10490920
scholarrs10490920
googlers10490920
pharmgkbrs10490920
gwascentralrs10490920
openSNPrs10490920
23andMers10490920
SNPshotrs10490920
SNPdbers10490920
MSV3drs10490920
GWAS Ctlgrs10490920
GMAF0.1928
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[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 32583210] Association of genetic variations in phosphatase and tensin homolog (PTEN) gene with polycystic ovary syndrome in South Indian women: a case control study.