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rs7865618

From SNPedia

Orientationplus
Stabilizedplus
Make rs7865618(A;A)
Make rs7865618(A;G)
Make rs7865618(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position22031006
GeneCDKN2B-AS1
is asnp
is mentioned by
dbSNPrs7865618
ebirs7865618
HLIrs7865618
Exacrs7865618
Varsomers7865618
Maprs7865618
PheGenIrs7865618
hapmaprs7865618
1000 genomesrs7865618
hgdprs7865618
ensemblrs7865618
gopubmedrs7865618
geneviewrs7865618
scholarrs7865618
googlers7865618
pharmgkbrs7865618
gwascentralrs7865618
openSNPrs7865618
23andMers7865618
23andMe allrs7865618
SNP Nexus

SNPshotrs7865618
SNPdbers7865618
MSV3drs7865618
GWAS Ctlgrs7865618
GMAF0.2094
Max Magnitude
? (A;A) (A;G) (G;G) 28
Rs7865618
PubMed [PMID 17634449OA-icon.png]
Affy Probeset SNP_A-1948244
Affy Orientation same
On GW 5.0 1
Alleles A/B A/G
Ancestral A
Population Caucasian
Allele A
Case Freq. 0.61
Control Freq. 0.55
Odds Ratio Het 1.23
Odds Ratio Hom 1.57
Odds Ratio All 1.26
Disease Coronary artery disease (CAD)


rs7865618 increases susceptibility to Coronary artery disease 1.23 times for heterozygotes (AG) and 1.57 times for homozygotes (AA) [PMID 17634449OA-icon.png]


[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 19926059] No association of chromosome 9p21.3 variation with clinical and angiographic outcomes after placement of drug-eluting stents


[PMID 21511257] The chromosome 9p21 region and myocardial infarction in a European population

GWAS snp
PMID [PMID 21606135OA-icon.png]
Trait
Title A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease.
Risk Allele A
P-val 2E-27
Odds Ratio 1.1800 [1.14-1.21]
GWAS snp
PMID [PMID 22428042OA-icon.png]
Trait
Title Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.
Risk Allele A
P-val 9E-11
Odds Ratio 1.7800 None


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


[PMID 24820060] Association between Polymorphisms rs1333040 and rs7865618 of Chromosome 9p21 and Sporadic Brain Arteriovenous Malformations