rs1780050
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1780050(G;G) |
| Make rs1780050(G;T) |
| Make rs1780050(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 77934855 |
| Gene | NEXN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1780050 |
| dbSNP (classic) | rs1780050 |
| ClinGen | rs1780050 |
| ebi | rs1780050 |
| HLI | rs1780050 |
| Exac | rs1780050 |
| Gnomad | rs1780050 |
| Varsome | rs1780050 |
| LitVar | rs1780050 |
| Map | rs1780050 |
| PheGenI | rs1780050 |
| Biobank | rs1780050 |
| 1000 genomes | rs1780050 |
| hgdp | rs1780050 |
| ensembl | rs1780050 |
| geneview | rs1780050 |
| scholar | rs1780050 |
| rs1780050 | |
| pharmgkb | rs1780050 |
| gwascentral | rs1780050 |
| openSNP | rs1780050 |
| 23andMe | rs1780050 |
| SNPshot | rs1780050 |
| SNPdbe | rs1780050 |
| MSV3d | rs1780050 |
| GWAS Ctlg | rs1780050 |
| GMAF | 0.4068 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24349201
] NEXN Is a Novel Susceptibility Gene for Coronary Artery Disease in Han Chinese
