ULK4, unc-51 like kinase 4, 54986

N. diseases: 32; N. variants: 515
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: rs114714860
rs114714860 		3 41841413 intron variant G/C snv 0.33
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs116837984
rs116837984 		3 41353856 intron variant T/A snv 8.5E-04
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs147428270
rs147428270 		3 41827229 intron variant T/C snv 0.27
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs148560677
rs148560677 		3 41405099 intron variant T/C snv 4.9E-05
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs188003336
rs188003336 		3 41396140 intron variant A/G snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs60257661
rs60257661 		3 41376349 intron variant A/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs7627367
rs7627367 		3 41569737 intron variant T/G snv 0.56
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2011 2011
dbSNP: rs79211428
rs79211428 		3 41880318 intron variant C/T snv 0.19
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs79211428
rs79211428 		3 41880318 intron variant C/T snv 0.19
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9816029
rs9816029 		3 41269871 intron variant G/C snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs6763508
rs6763508 		0.851 0.160 3 41709497 intron variant T/C snv 0.30
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.800 1.000 2 2011 2017
dbSNP: rs6763508
rs6763508 		0.851 0.160 3 41709497 intron variant T/C snv 0.30
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs6763508
rs6763508 		0.851 0.160 3 41709497 intron variant T/C snv 0.30
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs6763508
rs6763508 		0.851 0.160 3 41709497 intron variant T/C snv 0.30
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs73071352
rs73071352 		0.882 0.160 3 41786808 intron variant A/G snv 0.12
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.800 1.000 2 2011 2015
dbSNP: rs73071352
rs73071352 		0.882 0.160 3 41786808 intron variant A/G snv 0.12
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias 		Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs73071352
rs73071352 		0.882 0.160 3 41786808 intron variant A/G snv 0.12
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
Monoclonal Gammopathy of Undetermined Significance 		Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs9848754
rs9848754 		0.882 0.160 3 41712155 intron variant C/T snv 0.18
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
Monoclonal Gammopathy of Undetermined Significance 		Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9848754
rs9848754 		0.882 0.160 3 41712155 intron variant C/T snv 0.18
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias 		Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9848754
rs9848754 		0.882 0.160 3 41712155 intron variant C/T snv 0.18
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1052501
rs1052501 		0.925 0.160 3 41883906 missense variant C/G;T snv 0.80
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.810 1.000 3 2011 2014
dbSNP: rs9815354
rs9815354 		0.925 0.160 3 41871159 intron variant G/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 3 2009 2017
dbSNP: rs1052501
rs1052501 		0.925 0.160 3 41883906 missense variant C/G;T snv 0.80
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
Monoclonal Gammopathy of Undetermined Significance 		Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9815354
rs9815354 		0.925 0.160 3 41871159 intron variant G/A;T snv
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2009 2009
dbSNP: rs9815354
rs9815354 		0.925 0.160 3 41871159 intron variant G/A;T snv
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2011 2011