KLF12, Kruppel like factor 12, 11278

N. diseases: 58; N. variants: 20
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4454843
rs4454843
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7329599
rs7329599
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7335976
rs7335976
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7995668
rs7995668
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9600233
rs9600233
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2025424
rs2025424
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs2025424
rs2025424
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs35185444
rs35185444
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
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: rs7995760
rs7995760
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs7995760
rs7995760
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs58598658
rs58598658
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0236664
Disease:
Alcohol-Related Disorders 		C 0.700 GeneticVariation GWASCAT Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression. 29071344 2017
dbSNP: rs58598658
rs58598658
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1269683
Disease:
Major Depressive Disorder 		C 0.700 GeneticVariation GWASCAT Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression. 29071344 2017
dbSNP: rs58598658
rs58598658
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic 		C 0.700 GeneticVariation GWASCAT Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression. 29071344 2017
dbSNP: rs58598658
rs58598658
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0236970
Disease:
Alcohol-Induced Disorders 		C 0.700 GeneticVariation GWASCAT Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression. 29071344 2017
dbSNP: rs1886512
rs1886512
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0429097
Disease:
QRS complex feature 		0.700 GeneticVariation GWASCAT 52 Genetic Loci Influencing Myocardial Mass. 27659466 2016
dbSNP: rs66504755
rs66504755
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0200635
Disease:
Lymphocyte Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs728926
rs728926
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0429097
Disease:
QRS complex feature 		0.700 GeneticVariation GWASCAT 52 Genetic Loci Influencing Myocardial Mass. 27659466 2016
dbSNP: rs9318213
rs9318213
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1863416
Disease:
Autosomal dominant compelling helio ophthalmic outburst syndrome 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs12877581
rs12877581
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0036341
Disease:
Schizophrenia 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
dbSNP: rs1324913
rs1324913
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1314691
Disease:
Age at menarche 		G 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs728926
rs728926
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0429028
Disease:
QT interval feature (observable entity) 		T 0.700 GeneticVariation GWASCAT Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. 24952745 2014
dbSNP: rs12429889
rs12429889
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0085298
Disease:
Sudden Cardiac Death 		0.700 GeneticVariation GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
dbSNP: rs12429889
rs12429889
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C1720824
Disease:
Sudden Cardiac Arrest 		0.700 GeneticVariation GWASDB GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
dbSNP: rs1886512
rs1886512
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0018803
Disease:
Heart Function Tests 		A 0.700 GeneticVariation GWASCAT Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. 21076409 2010
dbSNP: rs2325562
rs2325562
Entrez Id: 11278
Gene Symbol: KLF12
KLF12
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009