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: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2015 2017
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2013 2017
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.020 1.000 2 2015 2015
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.020 1.000 2 2013 2017
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0342953
Disease: Organ dysfunction syndrome
Organ dysfunction syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C1277187
Disease: Left ventricular systolic dysfunction
Left ventricular systolic dysfunction 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0024138
Disease: Lupus Erythematosus, Discoid
Lupus Erythematosus, Discoid 		Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia 		Hemic and Lymphatic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2019 2019
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0024131
Disease: Lupus Vulgaris
Lupus Vulgaris 		Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1800625
rs1800625 		0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		Cardiovascular Diseases 0.010 1.000 1 2012 2012