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rs39453

From SNPedia

Orientationplus
Stabilizedplus
Make rs39453(C;C)
Make rs39453(C;T)
Make rs39453(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position25094230
is asnp
is mentioned by
dbSNPrs39453
ebirs39453
HLIrs39453
Exacrs39453
Varsomers39453
Maprs39453
PheGenIrs39453
hapmaprs39453
1000 genomesrs39453
hgdprs39453
ensemblrs39453
gopubmedrs39453
geneviewrs39453
scholarrs39453
googlers39453
pharmgkbrs39453
gwascentralrs39453
openSNPrs39453
23andMers39453
23andMe allrs39453
SNP Nexus

SNPshotrs39453
SNPdbers39453
MSV3drs39453
GWAS Ctlgrs39453
GMAF0.3136
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23300701OA-icon.png]
Trait Colorectal cancer
Title Genome-wide search for gene-gene interactions in colorectal cancer.
Risk Allele
P-val 2E-6
Odds Ratio 1.28 [1.16-1.43]