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: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.100 0.969 196 2009 2019
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		Digestive System Diseases; Infections 0.900 1.000 41 2009 2020
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		Nutritional and Metabolic Diseases 0.100 1.000 20 2010 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.100 0.947 19 2011 2019
dbSNP: rs368234815
rs368234815 		0.742 0.280 19 39248514 frameshift variant TT/G;T delins
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.100 1.000 18 2014 2019
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.100 1.000 14 2011 2018
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		Pathological Conditions, Signs and Symptoms 0.100 1.000 12 2011 2018
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.100 1.000 11 2010 2019
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.100 0.818 11 2012 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		Digestive System Diseases 0.080 0.875 8 2011 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
Human immunodeficiency virus (HIV) II infection category B1 		0.060 1.000 6 2010 2018
dbSNP: rs368234815
rs368234815 		0.742 0.280 19 39248514 frameshift variant TT/G;T delins
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		Digestive System Diseases; Infections 0.060 1.000 6 2014 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0023895
Disease: Liver diseases
Liver diseases 		Digestive System Diseases 0.050 1.000 5 2011 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		Digestive System Diseases; Infections 0.050 1.000 5 2012 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.040 1.000 4 2013 2019
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019158
Disease: Hepatitis
Hepatitis 		Digestive System Diseases 0.040 0.750 4 2011 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C4049392
Disease: Chronic hepatitis C genotype 1
Chronic hepatitis C genotype 1 		0.040 1.000 4 2011 2014
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections 		Infections 0.040 0.750 4 2014 2019
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.030 1.000 3 2013 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		Endocrine System Diseases 0.030 1.000 3 2011 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019189
Disease: Hepatitis, Chronic
Hepatitis, Chronic 		Digestive System Diseases 0.030 1.000 3 2016 2018
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 2013 2015
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0220766
Disease: Congenital hypoplasia of adrenal gland
Congenital hypoplasia of adrenal gland 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases 0.030 1.000 3 2011 2017
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C4505456
Disease: HIV Coinfection
HIV Coinfection 		Infections; Immune System Diseases 0.030 1.000 3 2013 2014
dbSNP: rs12979860
rs12979860 		0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection 		Digestive System Diseases; Infections 0.030 1.000 3 2014 2017