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: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2016 2016
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
Triple Negative Breast Neoplasms 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		Neoplasms 0.010 1.000 1 2014 2014
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
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 0.500 2 2013 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.020 1.000 2 2016 2016
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood 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: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		Neoplasms; Nervous System Diseases 0.020 1.000 2 2019 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		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: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2017 2019