rs121913527
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs121913527(A;A) |
| Make rs121913527(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 12 |
| Position | 25225628 |
| Gene | KRAS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121913527 |
| dbSNP (classic) | rs121913527 |
| ClinGen | rs121913527 |
| ebi | rs121913527 |
| HLI | rs121913527 |
| Exac | rs121913527 |
| Gnomad | rs121913527 |
| Varsome | rs121913527 |
| LitVar | rs121913527 |
| Map | rs121913527 |
| PheGenI | rs121913527 |
| Biobank | rs121913527 |
| 1000 genomes | rs121913527 |
| hgdp | rs121913527 |
| ensembl | rs121913527 |
| geneview | rs121913527 |
| scholar | rs121913527 |
| rs121913527 | |
| pharmgkb | rs121913527 |
| gwascentral | rs121913527 |
| openSNP | rs121913527 |
| 23andMe | rs121913527 |
| SNPshot | rs121913527 |
| SNPdbe | rs121913527 |
| MSV3d | rs121913527 |
| GWAS Ctlg | rs121913527 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121913527(A;A) rs121913527(C;C) rs121913527(T;T) |
| Alt | rs121913527(A;A) rs121913527(C;C) rs121913527(T;T) |
| Reference | Rs121913527(G;G) |
| Significance | Pathogenic |
| Disease | Rasopathy Colorectal Neoplasms not specified |
| Variation | info |
| Gene | KRAS |
| CLNDBN | Rasopathy Colorectal Neoplasms not specified |
| Reversed | 1 |
| HGVS | NC_000012.11:g.25378562C>A; NC_000012.11:g.25378562C>G; NC_000012.11:g.25378562C>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000473918.1, RCV000444020.1, RCV000178223.1, RCV000426420.1, |
