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rs4775302

From SNPedia

Orientationplus
Stabilizedplus
Make rs4775302(A;A)
Make rs4775302(A;G)
Make rs4775302(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position46347610
is asnp
is mentioned by
dbSNPrs4775302
ebirs4775302
HLIrs4775302
Exacrs4775302
Varsomers4775302
Maprs4775302
PheGenIrs4775302
hapmaprs4775302
1000 genomesrs4775302
hgdprs4775302
ensemblrs4775302
gopubmedrs4775302
geneviewrs4775302
scholarrs4775302
googlers4775302
pharmgkbrs4775302
gwascentralrs4775302
openSNPrs4775302
23andMers4775302
23andMe allrs4775302
SNP Nexus

SNPshotrs4775302
SNPdbers4775302
MSV3drs4775302
GWAS Ctlgrs4775302
GMAF0.4293
Max Magnitude
? (A;A) (A;G) (G;G) 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.