rs39453
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs39453(C;C) |
Make rs39453(C;T) |
Make rs39453(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 25094230 |
is a | snp |
is | mentioned by |
dbSNP | rs39453 |
dbSNP (classic) | rs39453 |
ClinGen | rs39453 |
ebi | rs39453 |
HLI | rs39453 |
Exac | rs39453 |
Gnomad | rs39453 |
Varsome | rs39453 |
LitVar | rs39453 |
Map | rs39453 |
PheGenI | rs39453 |
Biobank | rs39453 |
1000 genomes | rs39453 |
hgdp | rs39453 |
ensembl | rs39453 |
geneview | rs39453 |
scholar | rs39453 |
rs39453 | |
pharmgkb | rs39453 |
gwascentral | rs39453 |
openSNP | rs39453 |
23andMe | rs39453 |
SNPshot | rs39453 |
SNPdbe | rs39453 |
MSV3d | rs39453 |
GWAS Ctlg | rs39453 |
GMAF | 0.3136 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23300701] |
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] |