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rs367615

From SNPedia

Orientationplus
Stabilizedplus
Make rs367615(C;C)
Make rs367615(C;T)
Make rs367615(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position109613236
is asnp
is mentioned by
dbSNPrs367615
ebirs367615
HLIrs367615
Exacrs367615
Varsomers367615
Maprs367615
PheGenIrs367615
hapmaprs367615
1000 genomesrs367615
hgdprs367615
ensemblrs367615
gopubmedrs367615
geneviewrs367615
scholarrs367615
googlers367615
pharmgkbrs367615
gwascentralrs367615
openSNPrs367615
23andMers367615
23andMe allrs367615
SNP Nexus

SNPshotrs367615
SNPdbers367615
MSV3drs367615
GWAS Ctlgrs367615
GMAF0.3131
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 4E-8
Odds Ratio 1.35 [1.20-1.49]