rs4686799
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4686799(C;C) |
| Make rs4686799(C;T) |
| Make rs4686799(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 186733447 |
| Gene | KNG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4686799 |
| dbSNP (classic) | rs4686799 |
| ClinGen | rs4686799 |
| ebi | rs4686799 |
| HLI | rs4686799 |
| Exac | rs4686799 |
| Gnomad | rs4686799 |
| Varsome | rs4686799 |
| LitVar | rs4686799 |
| Map | rs4686799 |
| PheGenI | rs4686799 |
| Biobank | rs4686799 |
| 1000 genomes | rs4686799 |
| hgdp | rs4686799 |
| ensembl | rs4686799 |
| geneview | rs4686799 |
| scholar | rs4686799 |
| rs4686799 | |
| pharmgkb | rs4686799 |
| gwascentral | rs4686799 |
| openSNP | rs4686799 |
| 23andMe | rs4686799 |
| SNPshot | rs4686799 |
| SNPdbe | rs4686799 |
| MSV3d | rs4686799 |
| GWAS Ctlg | rs4686799 |
| GMAF | 0.27 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19330902] Gender-specific association between the kininogen 1 gene variants and essential hypertension in Chinese Han population.
[PMID 19716087
] Genetic variation in angiotensin-converting enzyme-related pathways associated with sudden cardiac arrest risk.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
