rs701265
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs701265(A;G) |
| Make rs701265(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 152836568 |
| Gene | P2RY1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs701265 |
| dbSNP (classic) | rs701265 |
| ClinGen | rs701265 |
| ebi | rs701265 |
| HLI | rs701265 |
| Exac | rs701265 |
| Gnomad | rs701265 |
| Varsome | rs701265 |
| LitVar | rs701265 |
| Map | rs701265 |
| PheGenI | rs701265 |
| Biobank | rs701265 |
| 1000 genomes | rs701265 |
| hgdp | rs701265 |
| ensembl | rs701265 |
| geneview | rs701265 |
| scholar | rs701265 |
| rs701265 | |
| pharmgkb | rs701265 |
| gwascentral | rs701265 |
| openSNP | rs701265 |
| 23andMe | rs701265 |
| SNPshot | rs701265 |
| SNPdbe | rs701265 |
| MSV3d | rs701265 |
| GWAS Ctlg | rs701265 |
| GMAF | 0.3375 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22574824
] P2RY1 and P2RY12 polymorphisms and on-aspirin platelet reactivity in patients with coronary artery disease
[PMID 23828624] Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome.
