BCL2L13, BCL2 like 13, 23786

N. diseases: 18; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13058451
rs13058451
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4819618
rs4819618
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4819618
rs4819618
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs140179402
rs140179402
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0201968
Disease:
Cortisol Measurement 		0.700 GeneticVariation GWASCAT Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. 29551627 2018
dbSNP: rs140179402
rs140179402
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0264408
Disease:
Childhood asthma 		0.700 GeneticVariation GWASCAT Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. 29551627 2018
dbSNP: rs34891900
rs34891900
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0200638
Disease:
Eosinophil count procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs34891900
rs34891900
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0200633
Disease:
Neutrophil count (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs5013026
rs5013026
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0200633
Disease:
Neutrophil count (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs5747327
rs5747327
Entrez Id: 23786
Gene Symbol: BCL2L13
BCL2L13
CUI: C0857490
Disease:
Granulocyte count 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016