HHEX, hematopoietically expressed homeobox, 3087

N. diseases: 73; N. variants: 2
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11319879
rs11319879 		10 92693719 intron variant A/- delins 0.53
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs11319879
rs11319879 		10 92693719 intron variant A/- delins 0.53
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs1231813088
rs1231813088 		0.851 0.160 10 92690015 missense variant C/T snv
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1231813088
rs1231813088 		0.851 0.160 10 92690015 missense variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 < 0.001 1 2007 2007
dbSNP: rs1231813088
rs1231813088 		0.851 0.160 10 92690015 missense variant C/T snv
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1231813088
rs1231813088 		0.851 0.160 10 92690015 missense variant C/T snv
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.010 1.000 1 2007 2007