rs16857031
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs16857031(C;G) |
| Make rs16857031(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 162143120 |
| Gene | LOC105371475, NOS1AP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16857031 |
| dbSNP (classic) | rs16857031 |
| ClinGen | rs16857031 |
| ebi | rs16857031 |
| HLI | rs16857031 |
| Exac | rs16857031 |
| Gnomad | rs16857031 |
| Varsome | rs16857031 |
| LitVar | rs16857031 |
| Map | rs16857031 |
| PheGenI | rs16857031 |
| Biobank | rs16857031 |
| 1000 genomes | rs16857031 |
| hgdp | rs16857031 |
| ensembl | rs16857031 |
| geneview | rs16857031 |
| scholar | rs16857031 |
| rs16857031 | |
| pharmgkb | rs16857031 |
| gwascentral | rs16857031 |
| openSNP | rs16857031 |
| 23andMe | rs16857031 |
| SNPshot | rs16857031 |
| SNPdbe | rs16857031 |
| MSV3d | rs16857031 |
| GWAS Ctlg | rs16857031 |
| GMAF | 0.1997 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
23andMe blog Influences QT interval
| GWAS snp | |
|---|---|
| PMID | [PMID 19305408 ]
|
| Trait | QT interval |
| Title | Common variants at ten loci influence QT interval duation in the QTGEN Study |
| Risk Allele | G |
| P-val | 1E-34 |
| Odds Ratio | |
[PMID 26600494] Analysis of SNP (single nucleotide polymorphism) multiplex markers related to sudden cardiac death in Brazilian families
