rs2286194
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs2286194(A;A) |
| Make rs2286194(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 81726133 |
| Gene | HGF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2286194 |
| dbSNP (classic) | rs2286194 |
| ClinGen | rs2286194 |
| ebi | rs2286194 |
| HLI | rs2286194 |
| Exac | rs2286194 |
| Gnomad | rs2286194 |
| Varsome | rs2286194 |
| LitVar | rs2286194 |
| Map | rs2286194 |
| PheGenI | rs2286194 |
| Biobank | rs2286194 |
| 1000 genomes | rs2286194 |
| hgdp | rs2286194 |
| ensembl | rs2286194 |
| geneview | rs2286194 |
| scholar | rs2286194 |
| rs2286194 | |
| pharmgkb | rs2286194 |
| gwascentral | rs2286194 |
| openSNP | rs2286194 |
| 23andMe | rs2286194 |
| SNPshot | rs2286194 |
| SNPdbe | rs2286194 |
| MSV3d | rs2286194 |
| GWAS Ctlg | rs2286194 |
| GMAF | 0.1979 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19471602
] Hepatocyte growth factor and myopia: Genetic association analyses in a caucasian population
[PMID 19576567] Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
