HHEX, hematopoietically expressed homeobox, 3087

N. diseases: 73; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11319879
rs11319879
Entrez Id: 3087
Gene Symbol: HHEX
HHEX
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: rs11319879
rs11319879
Entrez Id: 3087
Gene Symbol: HHEX
HHEX
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: rs1231813088
rs1231813088
Entrez Id: 3087
Gene Symbol: HHEX
HHEX
CUI: C0686347
Disease:
Tardive Dyskinesia 		0.010 GeneticVariation BEFREE The Xhosa schizophrenia patient group with abnormal involuntary movements (n=54) and a subgroup with tardive dyskinesia (n=30) was found to significantly differ in Ala-9Val genotype frequency (P=0.008 and P=0.011 respectively) compared to the Xhosa schizophrenia patient group without abnormal involuntary movements (n=204). 17291655 2007
dbSNP: rs1231813088
rs1231813088
Entrez Id: 3087
Gene Symbol: HHEX
HHEX
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE These results do not support a major role of the MnSOD Ala-9Val polymorphism in the development of schizophrenia or symptom severity in the Xhosa population. 17291655 2007
dbSNP: rs1231813088
rs1231813088
Entrez Id: 3087
Gene Symbol: HHEX
HHEX
CUI: C3714760
Disease:
Drug-induced tardive dyskinesia 		0.010 GeneticVariation BEFREE The Xhosa schizophrenia patient group with abnormal involuntary movements (n=54) and a subgroup with tardive dyskinesia (n=30) was found to significantly differ in Ala-9Val genotype frequency (P=0.008 and P=0.011 respectively) compared to the Xhosa schizophrenia patient group without abnormal involuntary movements (n=204). 17291655 2007
dbSNP: rs1231813088
rs1231813088
Entrez Id: 3087
Gene Symbol: HHEX
HHEX
CUI: C0392702
Disease:
Abnormal involuntary movement 		0.010 GeneticVariation BEFREE The Xhosa schizophrenia patient group with abnormal involuntary movements (n=54) and a subgroup with tardive dyskinesia (n=30) was found to significantly differ in Ala-9Val genotype frequency (P=0.008 and P=0.011 respectively) compared to the Xhosa schizophrenia patient group without abnormal involuntary movements (n=204). 17291655 2007