rs1886449
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1886449(C;C) |
Make rs1886449(C;T) |
Make rs1886449(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 73357977 |
is a | snp |
is | mentioned by |
dbSNP | rs1886449 |
dbSNP (classic) | rs1886449 |
ClinGen | rs1886449 |
ebi | rs1886449 |
HLI | rs1886449 |
Exac | rs1886449 |
Gnomad | rs1886449 |
Varsome | rs1886449 |
LitVar | rs1886449 |
Map | rs1886449 |
PheGenI | rs1886449 |
Biobank | rs1886449 |
1000 genomes | rs1886449 |
hgdp | rs1886449 |
ensembl | rs1886449 |
geneview | rs1886449 |
scholar | rs1886449 |
rs1886449 | |
pharmgkb | rs1886449 |
gwascentral | rs1886449 |
openSNP | rs1886449 |
23andMe | rs1886449 |
SNPshot | rs1886449 |
SNPdbe | rs1886449 |
MSV3d | rs1886449 |
GWAS Ctlg | rs1886449 |
GMAF | 0.2181 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20686608] |
Trait | |
Title | Genome-wide association study of pancreatic cancer in Japanese population |
Risk Allele | A |
P-val | 0.000009 |
Odds Ratio | 1.51 [1.26-1.80] |