rs1487441
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1487441(A;A) |
| Make rs1487441(A;G) |
| Make rs1487441(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 6 |
| Position | 98106018 |
| Gene | LOC101927335 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1487441 |
| dbSNP (classic) | rs1487441 |
| ClinGen | rs1487441 |
| ebi | rs1487441 |
| HLI | rs1487441 |
| Exac | rs1487441 |
| Gnomad | rs1487441 |
| Varsome | rs1487441 |
| LitVar | rs1487441 |
| Map | rs1487441 |
| PheGenI | rs1487441 |
| Biobank | rs1487441 |
| 1000 genomes | rs1487441 |
| hgdp | rs1487441 |
| ensembl | rs1487441 |
| geneview | rs1487441 |
| scholar | rs1487441 |
| rs1487441 | |
| pharmgkb | rs1487441 |
| gwascentral | rs1487441 |
| openSNP | rs1487441 |
| 23andMe | rs1487441 |
| SNPshot | rs1487441 |
| SNPdbe | rs1487441 |
| MSV3d | rs1487441 |
| GWAS Ctlg | rs1487441 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 25201988
] Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
