LEF1, lymphoid enhancer binding factor 1, 51176

N. diseases: 211; N. variants: 13
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: rs2003869
rs2003869 		0.925 0.120 4 108105258 intron variant A/C;G;T snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 2 2013 2016
dbSNP: rs898518
rs898518 		0.925 0.120 4 108095668 intron variant C/A;T snv
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2013 2013
dbSNP: rs116711774
rs116711774 		4 108099646 intron variant G/A snv 9.1E-03
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs2003869
rs2003869 		0.925 0.120 4 108105258 intron variant A/C;G;T snv
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs67372037
rs67372037 		4 108099543 intron variant GTGTGT/-;GT;GTGT;GTGTGTGT delins 0.39
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs7665304
rs7665304 		4 108104223 intron variant A/C snv 0.53
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs7665304
rs7665304 		4 108104223 intron variant A/C snv 0.53
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs7668764
rs7668764 		4 108146742 intron variant G/T snv 0.52
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs7690934
rs7690934 		0.925 0.120 4 108104709 intron variant T/C snv 0.57
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: rs7690934
rs7690934 		0.925 0.120 4 108104709 intron variant T/C snv 0.57
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: rs898518
rs898518 		0.925 0.120 4 108095668 intron variant C/A;T snv
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs922168
rs922168 		4 108136248 intron variant C/T snv 0.27
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs369649181
rs369649181 		1.000 0.080 4 108163645 missense variant C/T snv 8.0E-06 3.5E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs1048060629
rs1048060629 		1.000 4 108163576 missense variant G/T snv 4.0E-06 7.0E-06
CUI: C4085595
Disease: AL-RAQAD SYNDROME
AL-RAQAD SYNDROME 		0.010 1.000 1 2008 2008
dbSNP: rs61752607
rs61752607 		1.000 0.120 4 108165124 missense variant C/A;T snv 8.2E-03 6.1E-03
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs769814612
rs769814612 		1.000 0.120 4 108167727 missense variant T/C snv 3.2E-05; 4.0E-06
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs76996680
rs76996680 		0.882 0.120 4 108163665 missense variant G/A snv 1.0E-03 3.4E-04
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs76996680
rs76996680 		0.882 0.120 4 108163665 missense variant G/A snv 1.0E-03 3.4E-04
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2015 2015
dbSNP: rs76996680
rs76996680 		0.882 0.120 4 108163665 missense variant G/A snv 1.0E-03 3.4E-04
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015