BTG4, BTG anti-proliferation factor 4, 54766

N. diseases: 9; 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: rs4938534
rs4938534 		0.925 0.080 11 111404408 intron variant G/A snv 0.56
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.810 1.000 2 2012 2017
dbSNP: rs4938534
rs4938534 		0.925 0.080 11 111404408 intron variant G/A snv 0.56
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.100 0.846 13 2014 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.100 0.833 12 2014 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.100 0.750 12 2011 2018
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.070 0.857 7 2013 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.060 1.000 6 2013 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.040 0.750 4 2014 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.040 0.750 4 2014 2018
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.040 0.750 4 2014 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.030 1.000 3 2016 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2013 2018
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
Malignant neoplasm of gastrointestinal tract 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2015 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		Digestive System Diseases; Neoplasms 0.020 0.500 2 2014 2015
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0279607
Disease: Adult Hepatocellular Carcinoma
Adult Hepatocellular Carcinoma 		Digestive System Diseases; Neoplasms 0.020 0.500 2 2014 2015
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 2013 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2013 2018
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 1.000 2 2014 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma 		Digestive System Diseases; Neoplasms 0.020 0.500 2 2014 2015
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma 		Neoplasms 0.020 1.000 2 2019 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.020 1.000 2 2013 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2017 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2016 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.020 1.000 2 2016 2017
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		Neoplasms; Endocrine System Diseases 0.020 1.000 2 2015 2018