MAP4, microtubule associated protein 4, 4134

N. diseases: 42; N. variants: 8
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: rs319690
rs319690 		3 47885994 intron variant T/C snv 0.39
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2017 2017
dbSNP: rs1060407
rs1060407 		3 47916547 missense variant G/A;T snv 4.0E-06; 0.29
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs145407011
rs145407011 		1.000 0.080 3 48024338 intron variant A/T snv 1.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs319690
rs319690 		3 47885994 intron variant T/C snv 0.39
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs319690
rs319690 		3 47885994 intron variant T/C snv 0.39
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2011 2011
dbSNP: rs319690
rs319690 		3 47885994 intron variant T/C snv 0.39
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs35979968
rs35979968 		3 48050845 intron variant C/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs62260764
rs62260764 		3 47949010 intron variant G/C snv 0.17
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs6442101
rs6442101 		3 48089403 upstream gene variant C/T snv 0.74
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs6442101
rs6442101 		3 48089403 upstream gene variant C/T snv 0.74
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs7429990
rs7429990 		1.000 0.040 3 47860313 intron variant C/A snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7429990
rs7429990 		1.000 0.040 3 47860313 intron variant C/A snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs9836027
rs9836027 		3 47892140 missense variant C/T snv 1.0E-02 4.6E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016