rs1926203
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1926203(G;G) |
| Make rs1926203(G;T) |
| Make rs1926203(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 88967577 |
| Gene | ACTA2, FAS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1926203 |
| dbSNP (classic) | rs1926203 |
| ClinGen | rs1926203 |
| ebi | rs1926203 |
| HLI | rs1926203 |
| Exac | rs1926203 |
| Gnomad | rs1926203 |
| Varsome | rs1926203 |
| LitVar | rs1926203 |
| Map | rs1926203 |
| PheGenI | rs1926203 |
| Biobank | rs1926203 |
| 1000 genomes | rs1926203 |
| hgdp | rs1926203 |
| ensembl | rs1926203 |
| geneview | rs1926203 |
| scholar | rs1926203 |
| rs1926203 | |
| pharmgkb | rs1926203 |
| gwascentral | rs1926203 |
| openSNP | rs1926203 |
| 23andMe | rs1926203 |
| SNPshot | rs1926203 |
| SNPdbe | rs1926203 |
| MSV3d | rs1926203 |
| GWAS Ctlg | rs1926203 |
| GMAF | 0.4601 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19654303
] Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study
[PMID 21303977] Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk.
