KLHL29, kelch like family member 29, 114818

N. diseases: 15; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs115697725
rs115697725
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs181430167
rs181430167
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT The most strongly associated variants were rs181430167 (p = 6.8 × 10<sup>-7</sup> ) for systolic BP and rs12991132 (p = 4.0 × 10<sup>-7</sup> ) for diastolic BP. 31469255 2019
dbSNP: rs1991083
rs1991083
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0424678
Disease:
Lean body mass 		0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs2551347
rs2551347
Entrez Id: 54454;114818
Gene Symbol: ATAD2B;KLHL29
ATAD2B;KLHL29
CUI: C0005612
Disease:
Birth Weight 		T 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs34668726
rs34668726
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4665624
rs4665624
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs72796106
rs72796106
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7586272
rs7586272
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11125163
rs11125163
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs34668726
rs34668726
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0525045
Disease:
Mood Disorders 		G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs34668726
rs34668726
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs4665630
rs4665630
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0014548
Disease:
Epilepsy, Generalized 		C 0.700 GeneticVariation GWASCAT Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. 30531953 2018
dbSNP: rs737665
rs737665
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs56262900
rs56262900
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0518015
Disease:
Hemoglobin measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs56262900
rs56262900
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs56262900
rs56262900
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0018935
Disease:
Hematocrit procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4665630
rs4665630
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0020538
Disease:
Hypertensive disease 		0.700 GeneticVariation GWASCAT Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282 2011
dbSNP: rs4665630
rs4665630
Entrez Id: 114818
Gene Symbol: KLHL29
KLHL29
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282 2011