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rs7044859

From SNPedia

Orientationplus
Stabilizedplus
Make rs7044859(A;A)
Make rs7044859(A;T)
Make rs7044859(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position22018782
GeneCDKN2B-AS1
is asnp
is mentioned by
dbSNPrs7044859
ebirs7044859
HLIrs7044859
Exacrs7044859
Varsomers7044859
Maprs7044859
PheGenIrs7044859
hapmaprs7044859
1000 genomesrs7044859
hgdprs7044859
ensemblrs7044859
gopubmedrs7044859
geneviewrs7044859
scholarrs7044859
googlers7044859
pharmgkbrs7044859
gwascentralrs7044859
openSNPrs7044859
23andMers7044859
23andMe allrs7044859
SNP Nexus

SNPshotrs7044859
SNPdbers7044859
MSV3drs7044859
GWAS Ctlgrs7044859
GMAF0.3783
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 17909067] Sporadic Medullary Thyroid Carcinoma. rs7044859 alters the binding of the transcription factor HNF1


[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 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.