FES, FES proto-oncogene, tyrosine kinase, 2242

N. diseases: 12; N. variants: 11
Source: GWASCAT ×
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: rs2521501
rs2521501 		0.925 0.080 15 90894158 intron variant A/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.800 1.000 1 2011 2011
dbSNP: rs4702
rs4702 		1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.720 1.000 5 2014 2019
dbSNP: rs2521501
rs2521501 		0.925 0.080 15 90894158 intron variant A/C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 7 2011 2019
dbSNP: rs2521501
rs2521501 		0.925 0.080 15 90894158 intron variant A/C;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 6 2011 2018
dbSNP: rs2521501
rs2521501 		0.925 0.080 15 90894158 intron variant A/C;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 2 2011 2018
dbSNP: rs4932373
rs4932373 		1.000 0.040 15 90886057 intron variant A/C snv 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs11539637
rs11539637 		1.000 0.040 15 90885060 synonymous variant C/G;T snv 8.1E-06; 0.59
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs12906125
rs12906125 		15 90884382 intron variant G/A snv 0.29
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2016 2016
dbSNP: rs138682554
rs138682554 		15 90884462 5 prime UTR variant G/A snv 1.5E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs138682554
rs138682554 		15 90884462 5 prime UTR variant G/A snv 1.5E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs1894400
rs1894400 		15 90885725 intron variant C/T snv 0.28
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1894400
rs1894400 		15 90885725 intron variant C/T snv 0.28
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1894400
rs1894400 		15 90885725 intron variant C/T snv 0.28
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1894400
rs1894400 		15 90885725 intron variant C/T snv 0.28
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1894400
rs1894400 		15 90885725 intron variant C/T snv 0.28
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2071382
rs2071382 		1.000 0.040 15 90884967 intron variant T/C snv 0.57
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2071382
rs2071382 		1.000 0.040 15 90884967 intron variant T/C snv 0.57
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs2521501
rs2521501 		0.925 0.080 15 90894158 intron variant A/C;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2521501
rs2521501 		0.925 0.080 15 90894158 intron variant A/C;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs35346340
rs35346340 		15 90884642 splice region variant G/A;C;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs35346340
rs35346340 		15 90884642 splice region variant G/A;C;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs4702
rs4702 		1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4702
rs4702 		1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs4932373
rs4932373 		1.000 0.040 15 90886057 intron variant A/C snv 0.25
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs7183988
rs7183988 		15 90885359 missense variant T/G snv 0.59 0.53
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019