rs10013040
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10013040(A;A) |
| Make rs10013040(A;C) |
| Make rs10013040(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 177309998 |
| Gene | NEIL3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10013040 |
| dbSNP (classic) | rs10013040 |
| ClinGen | rs10013040 |
| ebi | rs10013040 |
| HLI | rs10013040 |
| Exac | rs10013040 |
| Gnomad | rs10013040 |
| Varsome | rs10013040 |
| LitVar | rs10013040 |
| Map | rs10013040 |
| PheGenI | rs10013040 |
| Biobank | rs10013040 |
| 1000 genomes | rs10013040 |
| hgdp | rs10013040 |
| ensembl | rs10013040 |
| geneview | rs10013040 |
| scholar | rs10013040 |
| rs10013040 | |
| pharmgkb | rs10013040 |
| gwascentral | rs10013040 |
| openSNP | rs10013040 |
| 23andMe | rs10013040 |
| SNPshot | rs10013040 |
| SNPdbe | rs10013040 |
| MSV3d | rs10013040 |
| GWAS Ctlg | rs10013040 |
| Max Magnitude | 0 |
[PMID 25703835] Genetic variants in the DNA repair gene NEIL3 and the risk of myocardial infarction in a nested case-control study. The HUNT Study
