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rs10503733

From SNPedia

Orientationminus
Stabilizedminus
Make rs10503733(A;A)
Make rs10503733(A;C)
Make rs10503733(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position23676505
is asnp
is mentioned by
dbSNPrs10503733
ebirs10503733
HLIrs10503733
Exacrs10503733
Varsomers10503733
Maprs10503733
PheGenIrs10503733
hapmaprs10503733
1000 genomesrs10503733
hgdprs10503733
ensemblrs10503733
gopubmedrs10503733
geneviewrs10503733
scholarrs10503733
googlers10503733
pharmgkbrs10503733
gwascentralrs10503733
openSNPrs10503733
23andMers10503733
23andMe allrs10503733
SNP Nexus

SNPshotrs10503733
SNPdbers10503733
MSV3drs10503733
GWAS Ctlgrs10503733
GMAF0.2897
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22923026OA-icon.png]
Trait Prostate cancer
Title Evaluating genetic risk for prostate cancer among Japanese and Latinos.
Risk Allele T
P-val 8E-8
Odds Ratio 1.29 NR


[PMID 17903296OA-icon.png] Genome-wide association with bone mass and geometry in the Framingham Heart Study.