rs944797
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs944797(C;C) |
Make rs944797(C;T) |
Make rs944797(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 22115287 |
Gene | CDKN2B-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs944797 |
dbSNP (classic) | rs944797 |
ClinGen | rs944797 |
ebi | rs944797 |
HLI | rs944797 |
Exac | rs944797 |
Gnomad | rs944797 |
Varsome | rs944797 |
LitVar | rs944797 |
Map | rs944797 |
PheGenI | rs944797 |
Biobank | rs944797 |
1000 genomes | rs944797 |
hgdp | rs944797 |
ensembl | rs944797 |
geneview | rs944797 |
scholar | rs944797 |
rs944797 | |
pharmgkb | rs944797 |
gwascentral | rs944797 |
openSNP | rs944797 |
23andMe | rs944797 |
SNPshot | rs944797 |
SNPdbe | rs944797 |
MSV3d | rs944797 |
GWAS Ctlg | rs944797 |
GMAF | 0.4913 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21971053] |
Trait | |
Title | Genome-wide association study of coronary artery disease in the Japanese. |
Risk Allele | C |
P-val | 6E-16 |
Odds Ratio | 1.2500 [1.18-1.31] |
[PMID 19463184] Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease.