Rs10490920

From SNPedia
Jump to: navigation, search

Orientationplus
Make rs10490920(C;C)
Make rs10490920(C;T)
Make rs10490920(T;T)
ReferenceGRCh37 37.1/132
Chromosome10
Position89685643
GenePTEN
is asnp
is mentioned by
dbSNPrs10490920
Exacrs10490920
PheGenIrs10490920
nextbiors10490920
hapmaprs10490920
1000 genomesrs10490920
hgdprs10490920
ensemblrs10490920
gopubmedrs10490920
geneviewrs10490920
scholarrs10490920
googlers10490920
pharmgkbrs10490920
gwascentralrs10490920
openSNPrs10490920
23andMers10490920
23andMe allrs10490920
SNP Nexus

SNPshotrs10490920
SNPdbers10490920
MSV3drs10490920
GMAF0.1928
? (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.