rs2995300
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2995300(A;A) |
Make rs2995300(A;C) |
Make rs2995300(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 133263019 |
Gene | ADAM8 |
is a | snp |
is | mentioned by |
dbSNP | rs2995300 |
dbSNP (classic) | rs2995300 |
ClinGen | rs2995300 |
ebi | rs2995300 |
HLI | rs2995300 |
Exac | rs2995300 |
Gnomad | rs2995300 |
Varsome | rs2995300 |
LitVar | rs2995300 |
Map | rs2995300 |
PheGenI | rs2995300 |
Biobank | rs2995300 |
1000 genomes | rs2995300 |
hgdp | rs2995300 |
ensembl | rs2995300 |
geneview | rs2995300 |
scholar | rs2995300 |
rs2995300 | |
pharmgkb | rs2995300 |
gwascentral | rs2995300 |
openSNP | rs2995300 |
23andMe | rs2995300 |
SNPshot | rs2995300 |
SNPdbe | rs2995300 |
MSV3d | rs2995300 |
GWAS Ctlg | rs2995300 |
GMAF | 0.1538 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 21640993] Common variation in the ADAM8 gene affects serum sADAM8 concentrations and the risk of myocardial infarction in two independent cohorts