Rs10788165

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Orientationplus
Make rs10788165(G;G)
Make rs10788165(G;T)
Make rs10788165(T;T)
ReferenceGRCh37.p5 37.3/135
Chromosome10
Position123044214
is asnp
is mentioned by
dbSNPrs10788165
Exacrs10788165
PheGenIrs10788165
nextbiors10788165
hapmaprs10788165
1000 genomesrs10788165
hgdprs10788165
ensemblrs10788165
gopubmedrs10788165
geneviewrs10788165
scholarrs10788165
googlers10788165
pharmgkbrs10788165
gwascentralrs10788165
openSNPrs10788165
23andMers10788165
23andMe allrs10788165
SNP Nexus

SNPshotrs10788165
SNPdbers10788165
MSV3drs10788165
GMAF0.3347
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 22130093OA-icon.png] New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort


[PMID 20514297OA-icon.png] 2010 CUA Abstracts.


[PMID 22523086OA-icon.png] Gene variants in the angiogenesis pathway and prostate cancer.