rs2824292
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2824292(A;A) |
Make rs2824292(A;G) |
Make rs2824292(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 17414857 |
is a | snp |
is | mentioned by |
dbSNP | rs2824292 |
dbSNP (classic) | rs2824292 |
ClinGen | rs2824292 |
ebi | rs2824292 |
HLI | rs2824292 |
Exac | rs2824292 |
Gnomad | rs2824292 |
Varsome | rs2824292 |
LitVar | rs2824292 |
Map | rs2824292 |
PheGenI | rs2824292 |
Biobank | rs2824292 |
1000 genomes | rs2824292 |
hgdp | rs2824292 |
ensembl | rs2824292 |
geneview | rs2824292 |
scholar | rs2824292 |
rs2824292 | |
pharmgkb | rs2824292 |
gwascentral | rs2824292 |
openSNP | rs2824292 |
23andMe | rs2824292 |
SNPshot | rs2824292 |
SNPdbe | rs2824292 |
MSV3d | rs2824292 |
GWAS Ctlg | rs2824292 |
GMAF | 0.4559 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24291282] Coxsackie and adenovirus receptor (CAR) is a modifier of cardiac conduction and arrhythmia vulnerability in the setting of myocardial ischemia
[PMID 20622880] Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.
[PMID 21574885] No evidence for an association between the rs2824292 variant at chromosome 21q21 and ventricular fibrillation during acute myocardial infarction in a German population.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 21
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d