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rs9600079

From SNPedia

Orientationplus
Stabilizedplus
Make rs9600079(G;G)
Make rs9600079(G;T)
Make rs9600079(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position73154002
is asnp
is mentioned by
dbSNPrs9600079
dbSNP (classic)rs9600079
ClinGenrs9600079
ebirs9600079
HLIrs9600079
Exacrs9600079
Gnomadrs9600079
Varsomers9600079
LitVarrs9600079
Maprs9600079
PheGenIrs9600079
Biobankrs9600079
1000 genomesrs9600079
hgdprs9600079
ensemblrs9600079
geneviewrs9600079
scholarrs9600079
googlers9600079
pharmgkbrs9600079
gwascentralrs9600079
openSNPrs9600079
23andMers9600079
SNPshotrs9600079
SNPdbers9600079
MSV3drs9600079
GWAS Ctlgrs9600079
GMAF0.4394
Max Magnitude0
? (G;G) (G;T) (T;T) 28


GWAS snp
PMID [PMID 20676098]
Trait
Title Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population
Risk Allele T
P-val 3E-9
Odds Ratio 1.18 [1.12-1.24]


[PMID 22056501OA-icon.png] Replication of five prostate cancer loci identified in an Asian population - Results from the NCI Breast and Prostate Cancer Cohort Consortium (BPC3)


[PMID 22114074OA-icon.png] Replication and cumulative effects of GWAS-identified genetic variations for prostate cancer in Asians: a case-control study in the ChinaPCa consortium.


[PMID 23405784] [Susceptibility to prostate cancer in Han Chinese: single nucleotide polymorphism analysis of 1 667 cases]