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rs496892

From SNPedia

Orientationminus
Stabilizedplus
Make rs496892(A;A)
Make rs496892(A;G)
Make rs496892(G;G)
ReferenceGRCh38 38.1/142
Chromosome9
Position22024352
GeneCDKN2B-AS1
is asnp
is mentioned by
dbSNPrs496892
ebirs496892
HLIrs496892
Exacrs496892
Varsomers496892
Maprs496892
PheGenIrs496892
hapmaprs496892
1000 genomesrs496892
hgdprs496892
ensemblrs496892
gopubmedrs496892
geneviewrs496892
scholarrs496892
googlers496892
pharmgkbrs496892
gwascentralrs496892
openSNPrs496892
23andMers496892
23andMe allrs496892
SNP Nexus

SNPshotrs496892
SNPdbers496892
MSV3drs496892
GWAS Ctlgrs496892
GMAF0.3508
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 18675980OA-icon.png] Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes


[PMID 20696043OA-icon.png] Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort

[PMID 18362232OA-icon.png] Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

[PMID 19214202OA-icon.png] Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis.

[PMID 19475673OA-icon.png] Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.

[PMID 20386740OA-icon.png] Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.

[PMID 20395613] Confirmation of an association of single-nucleotide polymorphism rs1333040 on 9p21 with familial and sporadic intracranial aneurysms in Japanese patients.