Rs1395479
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1395479 |
| PheGenI | rs1395479 |
| nextbio | rs1395479 |
| hapmap | rs1395479 |
| 1000 genomes | rs1395479 |
| hgdp | rs1395479 |
| ensembl | rs1395479 |
| gopubmed | rs1395479 |
| geneview | rs1395479 |
| scholar | rs1395479 |
| rs1395479 | |
| pharmgkb | rs1395479 |
| gwascentral | rs1395479 |
| openSNP | rs1395479 |
| 23andMe | rs1395479 |
| 23andMe all | rs1395479 |
| SNP Nexus | |
| SNPshot | rs1395479 |
| SNPdbe | rs1395479 |
| MSV3d | rs1395479 |
| Chromosome | 4 |
| Orientation | plus |
| GMAF | 0.1877 |
| Position | 178318191 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1395479(A;A) |
| Make rs1395479(A;C) |
| Make rs1395479(C;C) |
| ? | (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 | |
| GET Evidence | |
|---|---|
| rs1395479 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.234375 |
| summary | |
