rs3917010
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3917010(A;A) |
Make rs3917010(A;C) |
Make rs3917010(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 100725310 |
Gene | VCAM1 |
is a | snp |
is | mentioned by |
dbSNP | rs3917010 |
dbSNP (classic) | rs3917010 |
ClinGen | rs3917010 |
ebi | rs3917010 |
HLI | rs3917010 |
Exac | rs3917010 |
Gnomad | rs3917010 |
Varsome | rs3917010 |
LitVar | rs3917010 |
Map | rs3917010 |
PheGenI | rs3917010 |
Biobank | rs3917010 |
1000 genomes | rs3917010 |
hgdp | rs3917010 |
ensembl | rs3917010 |
geneview | rs3917010 |
scholar | rs3917010 |
rs3917010 | |
pharmgkb | rs3917010 |
gwascentral | rs3917010 |
openSNP | rs3917010 |
23andMe | rs3917010 |
SNPshot | rs3917010 |
SNPdbe | rs3917010 |
MSV3d | rs3917010 |
GWAS Ctlg | rs3917010 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 26662939] Genotype/allelic combinations as potential predictors of myocardial infarction.