HLX, H2.0 like homeobox, 3142

N. diseases: 28; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11588625
rs11588625
Entrez Id: 3142
Gene Symbol: HLX
HLX
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12141189
rs12141189
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3738182
rs3738182
Entrez Id: 3142
Gene Symbol: HLX
HLX
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17597773
rs17597773
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
CUI: C1445957
Disease:
Serum total cholesterol measurement 		C 0.700 GeneticVariation GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809 2016
dbSNP: rs17597773
rs17597773
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
CUI: C0201657
Disease:
C-reactive protein measurement 		C 0.700 GeneticVariation GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809 2016
dbSNP: rs41369048
rs41369048
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
CUI: C0200638
Disease:
Eosinophil 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: rs41369048
rs41369048
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
CUI: C0200641
Disease:
Blood basophil count (lab test) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2184658
rs2184658
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
CUI: C0677607
Disease:
Hashimoto Disease 		0.010 GeneticVariation BEFREE We genotyped -1514T/C (rs17250932) and -1993T/C (rs4794067) polymorphisms of TBX21, - 742C/G polymorphism (rs2184658) of HLX and -1420G/A polymorphism (rs1269486) of GATA3 in genomic DNA samples from Japanese patients; 51 patients with severe Hashimoto's disease (HD), 39 with mild HD, 66 with intractable Graves' disease (GD), in whom remission was difficult to induce, 47 with GD in remission and 79 healthy volunteers. 22014209 2012
dbSNP: rs2184658
rs2184658
Entrez Id: 3142;100873924
Gene Symbol: HLX;HLX-AS1
HLX;HLX-AS1
CUI: C0018213
Disease:
Graves Disease 		0.010 GeneticVariation BEFREE We genotyped -1514T/C (rs17250932) and -1993T/C (rs4794067) polymorphisms of TBX21, - 742C/G polymorphism (rs2184658) of HLX and -1420G/A polymorphism (rs1269486) of GATA3 in genomic DNA samples from Japanese patients; 51 patients with severe Hashimoto's disease (HD), 39 with mild HD, 66 with intractable Graves' disease (GD), in whom remission was difficult to induce, 47 with GD in remission and 79 healthy volunteers. 22014209 2012