rs9985399
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs9985399(C;C) |
| Make rs9985399(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 39967143 |
| Gene | MYRIP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9985399 |
| dbSNP (classic) | rs9985399 |
| ClinGen | rs9985399 |
| ebi | rs9985399 |
| HLI | rs9985399 |
| Exac | rs9985399 |
| Gnomad | rs9985399 |
| Varsome | rs9985399 |
| LitVar | rs9985399 |
| Map | rs9985399 |
| PheGenI | rs9985399 |
| Biobank | rs9985399 |
| 1000 genomes | rs9985399 |
| hgdp | rs9985399 |
| ensembl | rs9985399 |
| geneview | rs9985399 |
| scholar | rs9985399 |
| rs9985399 | |
| pharmgkb | rs9985399 |
| gwascentral | rs9985399 |
| openSNP | rs9985399 |
| 23andMe | rs9985399 |
| SNPshot | rs9985399 |
| SNPdbe | rs9985399 |
| MSV3d | rs9985399 |
| GWAS Ctlg | rs9985399 |
| GMAF | 0.2259 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21130836 |
| Trait | |
| Title | Whole genome association scan for genetic polymorphisms influencing information processing speed |
| Risk Allele | T |
| P-val | 0.000009 |
| Odds Ratio | 0.2600 [0.14-0.38] unit decrease |
