MIR4435-2HG, MIR4435-2 host gene, 541471

N. diseases: 86; N. variants: 67
Disease: Eosinophil count procedure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1448187
rs1448187
Entrez Id: 541471
Gene Symbol: MIR4435-2HG
MIR4435-2HG
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs72836346
rs72836346
Entrez Id: 10018;55289;541471
Gene Symbol: BCL2L11;ACOXL;MIR4435-2HG
BCL2L11;ACOXL;MIR4435-2HG
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17484848
rs17484848
Entrez Id: 10018;541471
Gene Symbol: BCL2L11;MIR4435-2HG
BCL2L11;MIR4435-2HG
CUI: C0200638
Disease:
Eosinophil count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7578982
rs7578982
Entrez Id: 55289;541471
Gene Symbol: ACOXL;MIR4435-2HG
ACOXL;MIR4435-2HG
CUI: C0200638
Disease:
Eosinophil count procedure 		T 0.700 GeneticVariation GWASDB Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. 21738478 2011