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rs7126629

From SNPedia

Orientationplus
Stabilizedplus
Make rs7126629(A;A)
Make rs7126629(A;C)
Make rs7126629(C;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position2207722
is asnp
is mentioned by
dbSNPrs7126629
ebirs7126629
HLIrs7126629
Exacrs7126629
Varsomers7126629
Maprs7126629
PheGenIrs7126629
hapmaprs7126629
1000 genomesrs7126629
hgdprs7126629
ensemblrs7126629
gopubmedrs7126629
geneviewrs7126629
scholarrs7126629
googlers7126629
pharmgkbrs7126629
gwascentralrs7126629
openSNPrs7126629
23andMers7126629
23andMe allrs7126629
SNP Nexus

SNPshotrs7126629
SNPdbers7126629
MSV3drs7126629
GWAS Ctlgrs7126629
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24740154OA-icon.png]
Trait Prostate cancer (early onset)
Title Genome-wide association scan for variants associated with early-onset prostate cancer.
Risk Allele C
P-val 2E-8
Odds Ratio 1.44 [1.31-1.57]