OLFM4, olfactomedin 4, 10562

N. diseases: 89; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12552
rs12552
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
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: rs12552
rs12552
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		A 0.700 GeneticVariation GWASCAT Identification of common genetic risk variants for autism spectrum disorder. 30804558 2019
dbSNP: rs12552
rs12552
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1269683
Disease:
Major Depressive Disorder 		A 0.700 GeneticVariation GWASCAT Identification of common genetic risk variants for autism spectrum disorder. 30804558 2019
dbSNP: rs12552
rs12552
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1269683
Disease:
Major Depressive Disorder 		A 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: rs12552
rs12552
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1269683
Disease:
Major Depressive Disorder 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. 29700475 2018
dbSNP: rs8181889
rs8181889
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1269683
Disease:
Major Depressive Disorder 		A 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: rs12552
rs12552
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. 27479909 2016
dbSNP: rs9568797
rs9568797
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1862941
Disease:
Amyotrophic Lateral Sclerosis, Sporadic 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs9568797
rs9568797
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1842675
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs9568797
rs9568797
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C1862939
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014
dbSNP: rs9568797
rs9568797
Entrez Id: 10562
Gene Symbol: OLFM4
OLFM4
CUI: C3542025
Disease:
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation GWASCAT Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. 24529757 2014