CSK, C-terminal Src kinase, 1445

N. diseases: 91; 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: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 5 2009 2018
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 4 2011 2019
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2011
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 2 2009 2011
dbSNP: rs12439944
rs12439944 		1.000 0.080 15 74783309 intron variant G/A;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2017 2017
dbSNP: rs1350193
rs1350193 		15 74791940 intron variant G/C snv 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1350193
rs1350193 		15 74791940 intron variant G/C snv 0.67
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2011 2011
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2301249
rs2301249 		15 74800043 intron variant T/C snv 0.66
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2301249
rs2301249 		15 74800043 intron variant T/C snv 0.66
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2301249
rs2301249 		15 74800043 intron variant T/C snv 0.66
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs3784789
rs3784789 		15 74790211 intron variant C/G snv 0.44
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs8033381
rs8033381 		15 74788344 intron variant G/A snv 0.66
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.050 0.800 5 2012 2018
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1378942
rs1378942 		0.790 0.240 15 74785026 intron variant C/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2168518
rs2168518 		0.851 0.160 15 74788737 mature miRNA variant G/A snv 0.71 0.44
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2014 2014