ENSA, endosulfine alpha, 2029

N. diseases: 25; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11204677
rs11204677
Entrez Id: 2029;107985203
Gene Symbol: ENSA;LOC107985203
ENSA;LOC107985203
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs11204682
rs11204682
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11204682
rs11204682
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs11204682
rs11204682
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4970966
rs4970966
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0750880
Disease:
Monocyte count result 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs4970966
rs4970966
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0200637
Disease:
Monocyte count procedure 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs11204682
rs11204682
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0200641
Disease:
Blood basophil count (lab test) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11204682
rs11204682
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
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: rs12045807
rs12045807
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C3280795
Disease:
HYPOPLASTIC LEFT HEART SYNDROME 2 		C 0.700 GeneticVariation GWASCAT A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. 26965164 2016
dbSNP: rs12045807
rs12045807
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C4551854
Disease:
HYPOPLASTIC LEFT HEART SYNDROME 1 		C 0.700 GeneticVariation GWASCAT A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. 26965164 2016
dbSNP: rs4970966
rs4970966
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0200637
Disease:
Monocyte 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: rs4970966
rs4970966
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0750880
Disease:
Monocyte count result 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6681426
rs6681426
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0016529
Disease:
Forced expiratory volume function 		G 0.700 GeneticVariation GWASCAT Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. 26635082 2015
dbSNP: rs6681426
rs6681426
Entrez Id: 2029
Gene Symbol: ENSA
ENSA
CUI: C0042834
Disease:
Vital capacity 		G 0.700 GeneticVariation GWASCAT Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. 26635082 2015