Variant: rs4665630 

    present in Gene: KLHL29
    present in Chromosome: 2
    Position on Chromosome: 23675447
    Alleles of this Variant: C/T

rs4665630 in KLHL29 gene and Coronary heart disease PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

rs4665630 in KLHL29 gene and Epilepsy, Generalized PMID 30531953 2018 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies.

rs4665630 in KLHL29 gene and Hypertensive disease PMID 21347282 2011 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.