rs10849373
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10849373(A;A) |
| Make rs10849373(A;G) |
| Make rs10849373(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 631795 |
| Gene | LOC100049716, NINJ2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10849373 |
| dbSNP (classic) | rs10849373 |
| ClinGen | rs10849373 |
| ebi | rs10849373 |
| HLI | rs10849373 |
| Exac | rs10849373 |
| Gnomad | rs10849373 |
| Varsome | rs10849373 |
| LitVar | rs10849373 |
| Map | rs10849373 |
| PheGenI | rs10849373 |
| Biobank | rs10849373 |
| 1000 genomes | rs10849373 |
| hgdp | rs10849373 |
| ensembl | rs10849373 |
| geneview | rs10849373 |
| scholar | rs10849373 |
| rs10849373 | |
| pharmgkb | rs10849373 |
| gwascentral | rs10849373 |
| openSNP | rs10849373 |
| 23andMe | rs10849373 |
| SNPshot | rs10849373 |
| SNPdbe | rs10849373 |
| MSV3d | rs10849373 |
| GWAS Ctlg | rs10849373 |
| GMAF | 0.2544 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 21722921] NINJ2 polymorphism is associated with ischemic stroke in Chinese Han population
