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: C0023418
Disease: leukemia
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: C0268398
Disease: Familial lichen amyloidosis
Familial lichen amyloidosis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		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: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular 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: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		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: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		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: C0238301
Disease: Cancer of Nasopharynx
Cancer of Nasopharynx 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2016 2016
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
Triple-Negative Breast Carcinoma 		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: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases 		Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C1333001
Disease: Childhood Renal Cell Carcinoma
Childhood Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0017638
Disease: Glioma
Glioma 		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: C0349530
Disease: Early gastric cancer
Early gastric cancer 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular 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: C0153392
Disease: Malignant neoplasm of nasopharynx
Malignant neoplasm of nasopharynx 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma 		Neoplasms; Eye Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4938723
rs4938723 		0.574 0.680 11 111511840 intron variant T/C snv 0.32
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood 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: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		Eye 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: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.010 < 0.001 1 2019 2019