LRRC4C, leucine rich repeat containing 4C, 57689

N. diseases: 18; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2939756
rs2939756
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs10444280
rs10444280
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
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: rs4612793
rs4612793
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
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: rs4612793
rs4612793
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
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: rs729210
rs729210
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
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: rs998447
rs998447
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs11606250
rs11606250
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
CUI: C0027092
Disease:
Myopia 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs184852128
rs184852128
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs184852128
rs184852128
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
CUI: C3548479
Disease:
response to bronchodilator 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs4611189
rs4611189
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
CUI: C0684328
Disease:
Reasoning 		0.700 GeneticVariation GWASCAT Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. 21107309 2011
dbSNP: rs11604865
rs11604865
Entrez Id: 57689
Gene Symbol: LRRC4C
LRRC4C
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009