rs757556226
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs757556226(A;A) |
| Make rs757556226(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 20 |
| Position | 63488308 |
| Gene | EEF1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757556226 |
| dbSNP (classic) | rs757556226 |
| ClinGen | rs757556226 |
| ebi | rs757556226 |
| HLI | rs757556226 |
| Exac | rs757556226 |
| Gnomad | rs757556226 |
| Varsome | rs757556226 |
| LitVar | rs757556226 |
| Map | rs757556226 |
| PheGenI | rs757556226 |
| Biobank | rs757556226 |
| 1000 genomes | rs757556226 |
| hgdp | rs757556226 |
| ensembl | rs757556226 |
| geneview | rs757556226 |
| scholar | rs757556226 |
| rs757556226 | |
| pharmgkb | rs757556226 |
| gwascentral | rs757556226 |
| openSNP | rs757556226 |
| 23andMe | rs757556226 |
| SNPshot | rs757556226 |
| SNPdbe | rs757556226 |
| MSV3d | rs757556226 |
| GWAS Ctlg | rs757556226 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs757556226(A;A) |
| Alt | rs757556226(A;A) |
| Reference | Rs757556226(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | EEF1A2 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000020.10:g.62119661G>A |
| CLNSRC | |
| CLNACC | RCV000427894.1, |
