rs730880469
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (GAG;GAG) | 0 | common in clinvar |
| Make rs730880469(-;-) |
| Make rs730880469(-;GAG) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 12 |
| Position | 25227335 |
| Gene | KRAS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs730880469 |
| dbSNP (classic) | rs730880469 |
| ClinGen | rs730880469 |
| ebi | rs730880469 |
| HLI | rs730880469 |
| Exac | rs730880469 |
| Gnomad | rs730880469 |
| Varsome | rs730880469 |
| LitVar | rs730880469 |
| Map | rs730880469 |
| PheGenI | rs730880469 |
| Biobank | rs730880469 |
| 1000 genomes | rs730880469 |
| hgdp | rs730880469 |
| ensembl | rs730880469 |
| geneview | rs730880469 |
| scholar | rs730880469 |
| rs730880469 | |
| pharmgkb | rs730880469 |
| gwascentral | rs730880469 |
| openSNP | rs730880469 |
| 23andMe | rs730880469 |
| SNPshot | rs730880469 |
| SNPdbe | rs730880469 |
| MSV3d | rs730880469 |
| GWAS Ctlg | rs730880469 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs730880469(-;-) |
| Alt | rs730880469(-;-) |
| Reference | Rs730880469(GAG;GAG) |
| Significance | Probable-Pathogenic |
| Disease | Rasopathy |
| Variation | info |
| Gene | KRAS |
| CLNDBN | Rasopathy |
| Reversed | 1 |
| HGVS | NC_000012.11:g.25380269_25380271delCTC |
| CLNSRC | |
| CLNACC | RCV000157931.1, |
