{{Rsnum
|rsid=9289231
|Gene=KALRN
|Chromosome=3
|position=124055231
|Orientation=plus
|GMAF=0.1171
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=KALRN
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.9 | 14.2 | 85.0
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.9 | 99.1
| YRI | 12.9 | 40.8 | 46.3
| ASW | 12.3 | 21.1 | 66.7
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.9 | 99.1
| GIH | 0.0 | 15.8 | 84.2
| LWK | 14.5 | 44.5 | 40.9
| MEX | 0.0 | 17.2 | 82.8
| MKK | 12.2 | 39.7 | 48.1
| TSI | 0.0 | 22.5 | 77.5
| HapMapRevision=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|OA=1
}}

{{omim
|desc=CORONARY HEART DISEASE, SUSCEPTIBILITY TO, 5
|id=608901
|rsnum=9289231
}}

{{omim
|id=604605
|desc=KALIRIN; KALRN
|rsnum=9289231
}}
{{PMID Auto
|PMID=19706030
|Title=Validation Study of Genetic Associations with Coronary Artery Disease on Chromosome 3q13-21 and Potential Effect Modification by Smoking
|OA=1
}}

{{omim
|id=604605
|rsnum=9289231
|variant=0001
}}

{{PMID Auto
|PMID=18179892
|Title=Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
|OA=1
}}

{{ClinVar
|ALT=G
|CAF=0.8829; 0.1171
|CHROM=3
|CLNACC=RCV000005791.1
|CLNALLE=1
|CLNDBN=Coronary heart disease 5
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1837173:608901
|CLNHGVS=NC_000003.11:g.123774078T>G
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604605.0001
|COMMON=1
|Disease=Coronary heart disease 5
|FwdALT=G
|FwdREF=T
|REF=T
|RSPOS=123774078
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM
|VC=SNV
|VP=0x05016800000015051f110100
|WGT=0
|dbSNPBuildID=119
|rsid=9289231
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}