rs2070999
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2070999(A;A) |
| Make rs2070999(A;G) |
| Make rs2070999(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 2999495 |
| Gene | LOC105374888, NQO2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2070999 |
| dbSNP (classic) | rs2070999 |
| ClinGen | rs2070999 |
| ebi | rs2070999 |
| HLI | rs2070999 |
| Exac | rs2070999 |
| Gnomad | rs2070999 |
| Varsome | rs2070999 |
| LitVar | rs2070999 |
| Map | rs2070999 |
| PheGenI | rs2070999 |
| Biobank | rs2070999 |
| 1000 genomes | rs2070999 |
| hgdp | rs2070999 |
| ensembl | rs2070999 |
| geneview | rs2070999 |
| scholar | rs2070999 |
| rs2070999 | |
| pharmgkb | rs2070999 |
| gwascentral | rs2070999 |
| openSNP | rs2070999 |
| 23andMe | rs2070999 |
| SNPshot | rs2070999 |
| SNPdbe | rs2070999 |
| MSV3d | rs2070999 |
| GWAS Ctlg | rs2070999 |
| GMAF | 0.3007 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 24354914] NQO1 rs1800566 C>T polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population
[PMID 23054000] Genetic variants in metabolizing genes NQO1, NQO2, MTHFR and risk of prostate cancer: a study from North India.
