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rs10788165

From SNPedia

Orientationplus
Stabilizedplus
Make rs10788165(G;G)
Make rs10788165(G;T)
Make rs10788165(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position121284700
is asnp
is mentioned by
dbSNPrs10788165
dbSNP (classic)rs10788165
ClinGenrs10788165
ebirs10788165
HLIrs10788165
Exacrs10788165
Gnomadrs10788165
Varsomers10788165
LitVarrs10788165
Maprs10788165
PheGenIrs10788165
Biobankrs10788165
1000 genomesrs10788165
hgdprs10788165
ensemblrs10788165
geneviewrs10788165
scholarrs10788165
googlers10788165
pharmgkbrs10788165
gwascentralrs10788165
openSNPrs10788165
23andMers10788165
SNPshotrs10788165
SNPdbers10788165
MSV3drs10788165
GWAS Ctlgrs10788165
GMAF0.3347
Max Magnitude0
? (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.