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: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0015695
Disease: Fatty Liver
Fatty Liver 		Digestive System Diseases 0.020 1.000 2 2012 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0400914
Disease: Acute hepatitis C
Acute hepatitis C 		Digestive System Diseases; Infections 0.020 1.000 2 2012 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C3805156
Disease: Chronic hepatitis C virus genotype 1
Chronic hepatitis C virus genotype 1 		Digestive System Diseases; Infections 0.020 1.000 2 2012 2014
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0022346
Disease: Icterus
Icterus 		Pathological Conditions, Signs and Symptoms 0.020 1.000 2 2012 2019
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		Neoplasms 0.020 1.000 2 2013 2016
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0341439
Disease: Chronic liver disease
Chronic liver disease 		Digestive System Diseases 0.020 1.000 2 2014 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0543697
Disease: Mixed cryoglobulinemia
Mixed cryoglobulinemia 		Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.020 1.000 2 2015 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis 		Infections; Nervous System Diseases 0.020 1.000 2 2012 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C1608426
Disease: Compensated cirrhosis
Compensated cirrhosis 		0.020 1.000 2 2015 2016
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0006271
Disease: Bronchiolitis
Bronchiolitis 		Infections; Respiratory Tract Diseases 0.020 1.000 2 2012 2020
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019693
Disease: HIV Infections
HIV Infections 		Infections; Immune System Diseases 0.020 0.500 2 2010 2018
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		Infections 0.020 1.000 2 2010 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0002871
Disease: Anemia
Anemia 		Hemic and Lymphatic Diseases 0.020 1.000 2 2012 2020
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0005283
Disease: beta Thalassemia
beta Thalassemia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0524911
Disease: Hepatitis D, Chronic
Hepatitis D, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C3887641
Disease: Recurrent hepatitis
Recurrent hepatitis 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0021345
Disease: Infectious Mononucleosis
Infectious Mononucleosis 		Infections; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0020097
Disease: HTLV-I Infections
HTLV-I Infections 		Infections; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0022408
Disease: Arthropathy
Arthropathy 		Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019069
Disease: Hemophilia A
Hemophilia A 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019159
Disease: Hepatitis A
Hepatitis A 		Digestive System Diseases; Infections 0.010 1.000 1 2013 2013
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0020433
Disease: Hyperbilirubinemia
Hyperbilirubinemia 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019