rs7217186
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7217186(C;C) |
Make rs7217186(C;T) |
Make rs7217186(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 4636097 |
Gene | ALOX15 |
is a | snp |
is | mentioned by |
dbSNP | rs7217186 |
dbSNP (classic) | rs7217186 |
ClinGen | rs7217186 |
ebi | rs7217186 |
HLI | rs7217186 |
Exac | rs7217186 |
Gnomad | rs7217186 |
Varsome | rs7217186 |
LitVar | rs7217186 |
Map | rs7217186 |
PheGenI | rs7217186 |
Biobank | rs7217186 |
1000 genomes | rs7217186 |
hgdp | rs7217186 |
ensembl | rs7217186 |
geneview | rs7217186 |
scholar | rs7217186 |
rs7217186 | |
pharmgkb | rs7217186 |
gwascentral | rs7217186 |
openSNP | rs7217186 |
23andMe | rs7217186 |
SNPshot | rs7217186 |
SNPdbe | rs7217186 |
MSV3d | rs7217186 |
GWAS Ctlg | rs7217186 |
GMAF | 0.4729 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20676957] Two single nucleotide polymorphisms in ALOX15 are associated with risk of coronary artery disease in a Chinese Han population
[PMID 22351111] Association of ALOX15 gene polymorphism with ischemic stroke in Northern Chinese Han population.