MAPK4, mitogen-activated protein kinase 4, 5596

N. diseases: 19; N. variants: 9
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: rs1025686
rs1025686 		18 50620757 intron variant A/G snv 0.26
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs1025687
rs1025687 		18 50621423 intron variant T/C snv 0.61
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1025687
rs1025687 		18 50621423 intron variant T/C snv 0.61
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1025687
rs1025687 		18 50621423 intron variant T/C snv 0.61
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs1025688
rs1025688 		18 50621506 intron variant G/A snv 0.35
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs1025688
rs1025688 		18 50621506 intron variant G/A snv 0.35
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs1025688
rs1025688 		18 50621506 intron variant G/A snv 0.35
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs61148001
rs61148001 		18 50606871 intron variant C/T snv 0.23
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs745821
rs745821 		18 50616484 intron variant T/G snv 0.26
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs1893490
rs1893490 		1.000 0.040 18 50669431 non coding transcript exon variant T/C snv 0.48
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1893490
rs1893490 		1.000 0.040 18 50669431 non coding transcript exon variant T/C snv 0.48
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3752088
rs3752088 		1.000 0.040 18 50714891 intron variant C/A snv 0.51
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3752088
rs3752088 		1.000 0.040 18 50714891 intron variant C/A snv 0.51
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3794899
rs3794899 		1.000 0.040 18 50719733 intron variant C/T snv 0.81
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3794899
rs3794899 		1.000 0.040 18 50719733 intron variant C/T snv 0.81
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3892158
rs3892158 		1.000 0.040 18 50674143 intron variant C/T snv 0.69
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3892158
rs3892158 		1.000 0.040 18 50674143 intron variant C/T snv 0.69
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.010 1.000 1 2015 2015