rs4907479
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4907479(A;A) |
Make rs4907479(A;G) |
Make rs4907479(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 113004794 |
Gene | LOC107984591, MCF2L |
is a | snp |
is | mentioned by |
dbSNP | rs4907479 |
dbSNP (classic) | rs4907479 |
ClinGen | rs4907479 |
ebi | rs4907479 |
HLI | rs4907479 |
Exac | rs4907479 |
Gnomad | rs4907479 |
Varsome | rs4907479 |
LitVar | rs4907479 |
Map | rs4907479 |
PheGenI | rs4907479 |
Biobank | rs4907479 |
1000 genomes | rs4907479 |
hgdp | rs4907479 |
ensembl | rs4907479 |
geneview | rs4907479 |
scholar | rs4907479 |
rs4907479 | |
pharmgkb | rs4907479 |
gwascentral | rs4907479 |
openSNP | rs4907479 |
23andMe | rs4907479 |
SNPshot | rs4907479 |
SNPdbe | rs4907479 |
MSV3d | rs4907479 |
GWAS Ctlg | rs4907479 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24163127] |
Trait | Bladder cancer |
Title | Genome-wide association study identifies multiple loci associated with bladder cancer risk. |
Risk Allele | |
P-val | 3E-6 |
Odds Ratio | 1.13 [1.07-1.18] |