rs765556214
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs765556214(A;A) |
| Make rs765556214(A;G) |
| Make rs765556214(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 105933765 |
| Gene | GRIA4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs765556214 |
| dbSNP (classic) | rs765556214 |
| ClinGen | rs765556214 |
| ebi | rs765556214 |
| HLI | rs765556214 |
| Exac | rs765556214 |
| Gnomad | rs765556214 |
| Varsome | rs765556214 |
| LitVar | rs765556214 |
| Map | rs765556214 |
| PheGenI | rs765556214 |
| Biobank | rs765556214 |
| 1000 genomes | rs765556214 |
| hgdp | rs765556214 |
| ensembl | rs765556214 |
| geneview | rs765556214 |
| scholar | rs765556214 |
| rs765556214 | |
| pharmgkb | rs765556214 |
| gwascentral | rs765556214 |
| openSNP | rs765556214 |
| 23andMe | rs765556214 |
| SNPshot | rs765556214 |
| SNPdbe | rs765556214 |
| MSV3d | rs765556214 |
| GWAS Ctlg | rs765556214 |
| Max Magnitude | 0 |
aka NM_000829.3(GRIA4):c.2090G>C or (p.Arg697Pro)
OMIM pathogenic variant
