KLF2, Kruppel like factor 2, 10365

N. diseases: 132; N. variants: 3
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: rs11086029
rs11086029 		1.000 0.160 19 16327850 3 prime UTR variant T/A snv 0.78
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3745318
rs3745318 		1.000 0.080 19 16325451 missense variant T/C snv 0.75 0.82
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1392080411
rs1392080411 		0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1392080411
rs1392080411 		0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06
CUI: C0023443
Disease: Hairy Cell Leukemia
Hairy Cell Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1392080411
rs1392080411 		0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06
CUI: C4721414
Disease: Mantle cell lymphoma
Mantle cell lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1392080411
rs1392080411 		0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06
CUI: C0334633
Disease: Malignant lymphoma - lymphoplasmacytic
Malignant lymphoma - lymphoplasmacytic 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1392080411
rs1392080411 		0.827 0.160 19 16325934 missense variant C/T snv 7.0E-06
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3745318
rs3745318 		1.000 0.080 19 16325451 missense variant T/C snv 0.75 0.82
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 < 0.001 1 2006 2006