BAALC, BAALC binder of MAP3K1 and KLF4, 79870

N. diseases: 47; N. variants: 2
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: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2018 2018
dbSNP: rs12548629
rs12548629 		0.776 0.120 8 103189173 intron variant C/T snv 0.24
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2018 2018
dbSNP: rs62527607
rs62527607 		0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14
CUI: C0279583
Disease: Childhood T Acute Lymphoblastic Leukemia
Childhood T Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs62527607
rs62527607 		0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14
CUI: C1292769
Disease: Precursor B-cell lymphoblastic leukemia
Precursor B-cell lymphoblastic leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs62527607
rs62527607 		0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14
CUI: C0085669
Disease: Acute leukemia
Acute leukemia 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs62527607
rs62527607 		0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14
CUI: C0023485
Disease: Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs62527607
rs62527607 		0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017