rs2275725
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common on affy axiom data |
Make rs2275725(A;A) |
Make rs2275725(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 133275531 |
Gene | ADAM8 |
is a | snp |
is | mentioned by |
dbSNP | rs2275725 |
dbSNP (classic) | rs2275725 |
ClinGen | rs2275725 |
ebi | rs2275725 |
HLI | rs2275725 |
Exac | rs2275725 |
Gnomad | rs2275725 |
Varsome | rs2275725 |
LitVar | rs2275725 |
Map | rs2275725 |
PheGenI | rs2275725 |
Biobank | rs2275725 |
1000 genomes | rs2275725 |
hgdp | rs2275725 |
ensembl | rs2275725 |
geneview | rs2275725 |
scholar | rs2275725 |
rs2275725 | |
pharmgkb | rs2275725 |
gwascentral | rs2275725 |
openSNP | rs2275725 |
23andMe | rs2275725 |
SNPshot | rs2275725 |
SNPdbe | rs2275725 |
MSV3d | rs2275725 |
GWAS Ctlg | rs2275725 |
GMAF | 0.09183 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21640993] Common variation in the ADAM8 gene affects serum sADAM8 concentrations and the risk of myocardial infarction in two independent cohorts