RCOR1, REST corepressor 1, 23186

N. diseases: 2; N. variants: 6
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1190335
rs1190335
Entrez Id: 23186
Gene Symbol: RCOR1
RCOR1
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1190335
rs1190335
Entrez Id: 23186
Gene Symbol: RCOR1
RCOR1
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10132160
rs10132160
Entrez Id: 23186
Gene Symbol: RCOR1
RCOR1
CUI: C0032181
Disease:
Platelet Count measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs11382616
rs11382616
Entrez Id: 23186
Gene Symbol: RCOR1
RCOR1
CUI: C0032181
Disease:
Platelet Count measurement 		GC 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11627756
rs11627756
Entrez Id: 23186
Gene Symbol: RCOR1
RCOR1
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11628569
rs11628569
Entrez Id: 23186
Gene Symbol: RCOR1
RCOR1
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs754404879
rs754404879
Entrez Id: 23186
Gene Symbol: RCOR1
RCOR1
CUI: C0431399
Disease:
Familial aplasia of the vermis 		T 0.700 GeneticVariation CLINVAR Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity. 26489029 2016