rs1800805
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1800805(A;A) |
Make rs1800805(A;G) |
Make rs1800805(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 169632043 |
Gene | SELP |
is a | snp |
is | mentioned by |
dbSNP | rs1800805 |
dbSNP (classic) | rs1800805 |
ClinGen | rs1800805 |
ebi | rs1800805 |
HLI | rs1800805 |
Exac | rs1800805 |
Gnomad | rs1800805 |
Varsome | rs1800805 |
LitVar | rs1800805 |
Map | rs1800805 |
PheGenI | rs1800805 |
Biobank | rs1800805 |
1000 genomes | rs1800805 |
hgdp | rs1800805 |
ensembl | rs1800805 |
geneview | rs1800805 |
scholar | rs1800805 |
rs1800805 | |
pharmgkb | rs1800805 |
gwascentral | rs1800805 |
openSNP | rs1800805 |
23andMe | rs1800805 |
SNPshot | rs1800805 |
SNPdbe | rs1800805 |
MSV3d | rs1800805 |
GWAS Ctlg | rs1800805 |
GMAF | 0.2608 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24504449] SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis
[PMID 16820586] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.
[PMID 22192915] Common polymorphisms in the P-selectin gene in women with recurrent spontaneous abortions.