rs9660992
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9660992(A;A) |
| Make rs9660992(A;G) |
| Make rs9660992(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 1 |
| Position | 205280322 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9660992 |
| dbSNP (classic) | rs9660992 |
| ClinGen | rs9660992 |
| ebi | rs9660992 |
| HLI | rs9660992 |
| Exac | rs9660992 |
| Gnomad | rs9660992 |
| Varsome | rs9660992 |
| LitVar | rs9660992 |
| Map | rs9660992 |
| PheGenI | rs9660992 |
| Biobank | rs9660992 |
| 1000 genomes | rs9660992 |
| hgdp | rs9660992 |
| ensembl | rs9660992 |
| geneview | rs9660992 |
| scholar | rs9660992 |
| rs9660992 | |
| pharmgkb | rs9660992 |
| gwascentral | rs9660992 |
| openSNP | rs9660992 |
| 23andMe | rs9660992 |
| SNPshot | rs9660992 |
| SNPdbe | rs9660992 |
| MSV3d | rs9660992 |
| GWAS Ctlg | rs9660992 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24026423 ]
|
| Trait | Mean platelet volume |
| Title | A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. |
| Risk Allele | A |
| P-val | 3E-13 |
| Odds Ratio | .11 [NR] unit increase |
