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rs9982601

From SNPedia

Orientationplus
Stabilizedplus
Make rs9982601(C;C)
Make rs9982601(C;T)
Make rs9982601(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position34226827
is asnp
is mentioned by
dbSNPrs9982601
ebirs9982601
HLIrs9982601
Exacrs9982601
Varsomers9982601
Maprs9982601
PheGenIrs9982601
hapmaprs9982601
1000 genomesrs9982601
hgdprs9982601
ensemblrs9982601
gopubmedrs9982601
geneviewrs9982601
scholarrs9982601
googlers9982601
pharmgkbrs9982601
gwascentralrs9982601
openSNPrs9982601
23andMers9982601
23andMe allrs9982601
SNP Nexus

SNPshotrs9982601
SNPdbers9982601
MSV3drs9982601
GWAS Ctlgrs9982601
GMAF0.1088
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele T
P-val 3E-10
Odds Ratio 1.18 [1.12-1.24]
GWAS snp
PMID [PMID 21378990OA-icon.png]
Trait
Title Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele T
P-val 4E-10
Odds Ratio 1.1800 [1.12-1.24]
GWAS snp
PMID [PMID 19198609OA-icon.png]
Trait Myocardial infarction (early onset)
Title Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Risk Allele T
P-val 6E-11
Odds Ratio 1.20 [1.14-1.27]



Coronary Heart Disease


[PMID 23100282OA-icon.png] Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study.

[PMID 20835900OA-icon.png] Genetics of diabetes complications.

[PMID 19956433OA-icon.png] Genetics of coronary artery disease: focus on genome-wide association studies.


GET Evidence
rs9982601
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary