rs9266
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs9266(C;C) |
| Make rs9266(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 25209283 |
| Gene | KRAS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9266 |
| dbSNP (classic) | rs9266 |
| ClinGen | rs9266 |
| ebi | rs9266 |
| HLI | rs9266 |
| Exac | rs9266 |
| Gnomad | rs9266 |
| Varsome | rs9266 |
| LitVar | rs9266 |
| Map | rs9266 |
| PheGenI | rs9266 |
| Biobank | rs9266 |
| 1000 genomes | rs9266 |
| hgdp | rs9266 |
| ensembl | rs9266 |
| geneview | rs9266 |
| scholar | rs9266 |
| rs9266 | |
| pharmgkb | rs9266 |
| gwascentral | rs9266 |
| openSNP | rs9266 |
| 23andMe | rs9266 |
| SNPshot | rs9266 |
| SNPdbe | rs9266 |
| MSV3d | rs9266 |
| GWAS Ctlg | rs9266 |
| GMAF | 0.4458 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24552817
] Extensive sequence variation in the 3' untranslated region of the KRAS gene in lung and ovarian cancer cases
[PMID 18805939] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.
[PMID 26515332] KRAS polymorphisms are associated with survival of CRC in Chinese population
| ClinVar | |
|---|---|
| Risk | rs9266(C;C) |
| Alt | rs9266(C;C) |
| Reference | Rs9266(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Cardio-facio-cutaneous syndrome Noonan syndrome |
| Variation | info |
| Gene | KRAS |
| CLNDBN | Cardio-facio-cutaneous syndrome Noonan syndrome |
| Reversed | 1 |
| HGVS | NC_000012.11:g.25362217A>G |
| CLNSRC | |
| CLNACC | RCV000342340.1, RCV000398489.1, |
