rs10494373
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs10494373(A;C) |
| Make rs10494373(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 162649572 |
| Gene | DDR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10494373 |
| dbSNP (classic) | rs10494373 |
| ClinGen | rs10494373 |
| ebi | rs10494373 |
| HLI | rs10494373 |
| Exac | rs10494373 |
| Gnomad | rs10494373 |
| Varsome | rs10494373 |
| LitVar | rs10494373 |
| Map | rs10494373 |
| PheGenI | rs10494373 |
| Biobank | rs10494373 |
| 1000 genomes | rs10494373 |
| hgdp | rs10494373 |
| ensembl | rs10494373 |
| geneview | rs10494373 |
| scholar | rs10494373 |
| rs10494373 | |
| pharmgkb | rs10494373 |
| gwascentral | rs10494373 |
| openSNP | rs10494373 |
| 23andMe | rs10494373 |
| SNPshot | rs10494373 |
| SNPdbe | rs10494373 |
| MSV3d | rs10494373 |
| GWAS Ctlg | rs10494373 |
| GMAF | 0.05785 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 22504417
] Identification of common variants associated with human hippocampal and intracranial volumes.
