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: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.050 1.000 5 2011 2017
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.050 1.000 5 2011 2017
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.050 1.000 5 2011 2017
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.040 0.750 4 2010 2016
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.040 0.750 4 2016 2018
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.040 0.750 4 2010 2016
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.040 0.750 4 2010 2016
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.040 1.000 4 2010 2017
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 1.000 2 2013 2014
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2019
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.020 1.000 2 2016 2017
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 2007 2007
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2019
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2019
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 2007 2007
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		Neoplasms; Stomatognathic Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		Neoplasms; Stomatognathic Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0007107
Disease: Malignant neoplasm of larynx
Malignant neoplasm of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature 		Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0021364
Disease: Male infertility
Male infertility 		Male Urogenital Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0595989
Disease: Carcinoma of larynx
Carcinoma of larynx 		Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2016 2016
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs4646903
rs4646903 		0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C0264490
Disease: Acute respiratory failure
Acute respiratory failure 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Respiratory Tract Diseases 0.010 1.000 1 2013 2013