rs45525634
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs45525634(G;G) |
Make rs45525634(G;T) |
Make rs45525634(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 52316377 |
Gene | PTGER2 |
is a | snp |
is | mentioned by |
dbSNP | rs45525634 |
dbSNP (classic) | rs45525634 |
ClinGen | rs45525634 |
ebi | rs45525634 |
HLI | rs45525634 |
Exac | rs45525634 |
Gnomad | rs45525634 |
Varsome | rs45525634 |
LitVar | rs45525634 |
Map | rs45525634 |
PheGenI | rs45525634 |
Biobank | rs45525634 |
1000 genomes | rs45525634 |
hgdp | rs45525634 |
ensembl | rs45525634 |
geneview | rs45525634 |
scholar | rs45525634 |
rs45525634 | |
pharmgkb | rs45525634 |
gwascentral | rs45525634 |
openSNP | rs45525634 |
23andMe | rs45525634 |
SNPshot | rs45525634 |
SNPdbe | rs45525634 |
MSV3d | rs45525634 |
GWAS Ctlg | rs45525634 |
Max Magnitude | 0 |
[PMID 24908683] Genetic variation in prostaglandin synthesis and related pathways, NSAID use, and colorectal cancer risk in the Colon Cancer Family Registry