rs3217992
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1.24x increased myocardial infarction risk | |
(A;G) | 1.24x increased myocardial infarction risk | |
(G;G) | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 22003224 |
Gene | CDKN2B, CDKN2B-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs3217992 |
dbSNP (classic) | rs3217992 |
ClinGen | rs3217992 |
ebi | rs3217992 |
HLI | rs3217992 |
Exac | rs3217992 |
Gnomad | rs3217992 |
Varsome | rs3217992 |
LitVar | rs3217992 |
Map | rs3217992 |
PheGenI | rs3217992 |
Biobank | rs3217992 |
1000 genomes | rs3217992 |
hgdp | rs3217992 |
ensembl | rs3217992 |
geneview | rs3217992 |
scholar | rs3217992 |
rs3217992 | |
pharmgkb | rs3217992 |
gwascentral | rs3217992 |
openSNP | rs3217992 |
23andMe | rs3217992 |
SNPshot | rs3217992 |
SNPdbe | rs3217992 |
MSV3d | rs3217992 |
GWAS Ctlg | rs3217992 |
GMAF | 0.3595 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25814643] Genetic Variations in MicroRNA-Binding Sites Affect MicroRNA-Mediated Regulation of Several Genes Associated With Cardio-metabolic Phenotypes
rs3217992 is a SNP in the cyclin-dependent kinase inhibitor 2B CDKN2B gene. A study of 432 Han Chinese patients with myocardial infarctions concluded that male subjects carrying a rs3217992(A) allele were at 1.24x increased risk (for MI).[PMID 19272367]
[PMID 23202125] Large-scale association analysis identifies new risk loci for coronary artery disease.
[PMID 23111177] CDKN2B-AS1 Genotype-Glaucoma Feature Correlations in Primary Open-Angle Glaucoma Patients From the United States
[PMID 20386740] Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
[PMID 20978019] CDKN2BAS is associated with periodontitis in different European populations and is activated by bacterial infection
[PMID 19559344] Genetic variants on chromosome 9p21 and ischemic stroke in Chinese
[PMID 19258477] Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
[PMID 18174243] Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population.
[PMID 17459456] A common variant of the p16(INK4a) genetic region is associated with physical function in older people.
[PMID 27486979] Functional single nucleotide polymorphisms within the cyclin-dependent kinase inhibitor 2A/2B region affect pancreatic cancer risk.
[PMID 29228923] CDKN2BAS gene polymorphisms and the risk of intracranial aneurysm in the Chinese population.
[PMID 30774116] Functional Genetic Single-Nucleotide Polymorphisms (SNPs) in Cyclin-Dependent Kinase Inhibitor 2A/B (CDKN2A/B) Locus Are Associated with Risk and Prognosis of Osteosarcoma in Chinese Populations.
[PMID 31770616] ANRIL polymorphisms (rs1333049 and rs3217992) in relation to plasma CRP levels among in-patients with CHD.
- Is a snp
- In dbSNP
- SNPs on chromosome 9
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2d