rs9289231

plus

Geno	Mag	Summary
(T;T)	0

Make rs9289231(G;G)

Make rs9289231(G;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

124055231

Gene

KALRN

is a	snp
is	mentioned by
dbSNP	rs9289231
dbSNP (classic)	rs9289231
ClinGen	rs9289231
ebi	rs9289231
HLI	rs9289231
Exac	rs9289231
Gnomad	rs9289231
Varsome	rs9289231
LitVar	rs9289231
Map	rs9289231
PheGenI	rs9289231
Biobank	rs9289231
1000 genomes	rs9289231
hgdp	rs9289231
ensembl	rs9289231
geneview	rs9289231
scholar	rs9289231
google	rs9289231
pharmgkb	rs9289231
gwascentral	rs9289231
openSNP	rs9289231
23andMe	rs9289231
SNPshot	rs9289231
SNPdbe	rs9289231
MSV3d	rs9289231
GWAS Ctlg	rs9289231

GMAF

0.1171

Max Magnitude

0

?

(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 17357071 ]

OMIM	608901
Desc	CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 5
Variant
Related	also

OMIM	604605
Desc	KALIRIN; KALRN
Variant
Related	also

[PMID 19706030 ] Validation Study of Genetic Associations with Coronary Artery Disease on Chromosome 3q13-21 and Potential Effect Modification by Smoking

OMIM	604605
Desc
Variant	0001
Related	also

[PMID 18179892 ] 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,

[PMID 30483314 ] Association between Serum Kalirin Levels and the KALRN gene rs9289231 Polymorphism in Early-Onset Coronary Artery Disease.