rs6538697
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6538697(C;C) |
| Make rs6538697(C;T) |
| Make rs6538697(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 96009832 |
| Gene | LOC102723340, LTA4H |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6538697 |
| dbSNP (classic) | rs6538697 |
| ClinGen | rs6538697 |
| ebi | rs6538697 |
| HLI | rs6538697 |
| Exac | rs6538697 |
| Gnomad | rs6538697 |
| Varsome | rs6538697 |
| LitVar | rs6538697 |
| Map | rs6538697 |
| PheGenI | rs6538697 |
| Biobank | rs6538697 |
| 1000 genomes | rs6538697 |
| hgdp | rs6538697 |
| ensembl | rs6538697 |
| geneview | rs6538697 |
| scholar | rs6538697 |
| rs6538697 | |
| pharmgkb | rs6538697 |
| gwascentral | rs6538697 |
| openSNP | rs6538697 |
| 23andMe | rs6538697 |
| SNPshot | rs6538697 |
| SNPdbe | rs6538697 |
| MSV3d | rs6538697 |
| GWAS Ctlg | rs6538697 |
| GMAF | 0.1671 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 23079278] Genetic variation in members of the leukotrienes biosynthesis pathway confers risk of ischemic stroke in Eastern Han Chinese
[PMID 23324273] Association between genetic variants of the leukotriene biosynthesis pathway and the risk of stroke: a case-control study in the Chinese Han population
[PMID 19130089
] Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.
[PMID 25721704] Variants in ALOX5, ALOX5AP and LTA4H are not associated with atherosclerotic plaque phenotypes: The Athero-Express Genomics Study
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 12
- 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 HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
