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rs9289231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs9289231(G;G)
Make rs9289231(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position124055231
GeneKALRN
is asnp
is mentioned by
dbSNPrs9289231
ebirs9289231
HLIrs9289231
Exacrs9289231
Varsomers9289231
Maprs9289231
PheGenIrs9289231
hapmaprs9289231
1000 genomesrs9289231
hgdprs9289231
ensemblrs9289231
gopubmedrs9289231
geneviewrs9289231
scholarrs9289231
googlers9289231
pharmgkbrs9289231
gwascentralrs9289231
openSNPrs9289231
23andMers9289231
23andMe allrs9289231
SNP Nexus

SNPshotrs9289231
SNPdbers9289231
MSV3drs9289231
GWAS Ctlgrs9289231
GMAF0.1171
Max Magnitude0
? (G;G) (G;T) (T;T) 28
In a study of early onset coronary artery disease, rs9289231, the risk allele of this SNP, located in the kalirin KALRN gene, was associated with increased odds (OR 2.1), and also for increased atherosclerosis burden. [PMID 17357071OA-icon.png]
OMIM608901
DescCORONARY HEART DISEASE, SUSCEPTIBILITY TO, 5
Variant
Relatedalso
OMIM604605
DescKALIRIN; KALRN
Variant
Relatedalso
[PMID 19706030OA-icon.png] Validation Study of Genetic Associations with Coronary Artery Disease on Chromosome 3q13-21 and Potential Effect Modification by Smoking
OMIM604605
Desc
Variant0001
Relatedalso
[PMID 18179892OA-icon.png] Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.


ClinVar
Risk rs9289231(G;G)
Alt rs9289231(G;G)
Reference rs9289231(T;T)
Significance Other
Disease Coronary heart disease 5
Variation info
Gene KALRN
CLNDBN Coronary heart disease 5
Reversed 0
HGVS NC_000003.11:g.123774078T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005791.2,