ELOVL7, ELOVL fatty acid elongase 7, 79993

N. diseases: 13; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4700393
rs4700393
Entrez Id: 79993
Gene Symbol: ELOVL7
ELOVL7
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs4700393
rs4700393
Entrez Id: 79993
Gene Symbol: ELOVL7
ELOVL7
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: rs4700394
rs4700394
Entrez Id: 79993
Gene Symbol: ELOVL7
ELOVL7
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs6449502
rs6449502
Entrez Id: 79993
Gene Symbol: ELOVL7
ELOVL7
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7715147
rs7715147
Entrez Id: 79993
Gene Symbol: ELOVL7
ELOVL7
CUI: C0037019
Disease:
Shy-Drager Syndrome 		C 0.700 GeneticVariation GWASCAT A genome-wide association study in multiple system atrophy. 27629089 2016
dbSNP: rs7715147
rs7715147
Entrez Id: 79993
Gene Symbol: ELOVL7
ELOVL7
CUI: C0393571
Disease:
Multiple System Atrophy 		C 0.700 GeneticVariation GWASCAT A genome-wide association study in multiple system atrophy. 27629089 2016