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rs10749408

From SNPedia

Orientationplus
Stabilizedplus
Make rs10749408(C;C)
Make rs10749408(C;T)
Make rs10749408(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position121208012
is asnp
is mentioned by
dbSNPrs10749408
dbSNP (classic)rs10749408
ClinGenrs10749408
ebirs10749408
HLIrs10749408
Exacrs10749408
Gnomadrs10749408
Varsomers10749408
LitVarrs10749408
Maprs10749408
PheGenIrs10749408
Biobankrs10749408
1000 genomesrs10749408
hgdprs10749408
ensemblrs10749408
geneviewrs10749408
scholarrs10749408
googlers10749408
pharmgkbrs10749408
gwascentralrs10749408
openSNPrs10749408
23andMers10749408
SNPshotrs10749408
SNPdbers10749408
MSV3drs10749408
GWAS Ctlgrs10749408
GMAF0.2585
Max Magnitude0
? (C;C) (C;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.