rs1395479
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1395479(A;A) |
| Make rs1395479(A;C) |
| Make rs1395479(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 177397037 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1395479 |
| dbSNP (classic) | rs1395479 |
| ClinGen | rs1395479 |
| ebi | rs1395479 |
| HLI | rs1395479 |
| Exac | rs1395479 |
| Gnomad | rs1395479 |
| Varsome | rs1395479 |
| LitVar | rs1395479 |
| Map | rs1395479 |
| PheGenI | rs1395479 |
| Biobank | rs1395479 |
| 1000 genomes | rs1395479 |
| hgdp | rs1395479 |
| ensembl | rs1395479 |
| geneview | rs1395479 |
| scholar | rs1395479 |
| rs1395479 | |
| pharmgkb | rs1395479 |
| gwascentral | rs1395479 |
| openSNP | rs1395479 |
| 23andMe | rs1395479 |
| SNPshot | rs1395479 |
| SNPdbe | rs1395479 |
| MSV3d | rs1395479 |
| GWAS Ctlg | rs1395479 |
| GMAF | 0.1882 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs1395479 |
| PubMedID | [PMID 17903306 ]
|
| Condition | Heart rate variability traits |
| Gene | NEIL3 |
| Risk Allele | |
| pValue | 7.00E-006 |
| OR | NA |
| 95% CI | |
| GWAS snp | |
|---|---|
| PMID | [PMID 23698163]
|
| Trait | Serum selenium levels |
| Title | Genome-wide association study of serum selenium concentrations. |
| Risk Allele | A |
| P-val | 3E-7 |
| Odds Ratio | .04 [0.027-0.059] mg/dL increase |
[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
