Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		0.900 1.000 41 2009 2020
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.100 0.969 196 2009 2019
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		0.100 1.000 20 2010 2017
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.100 0.947 19 2011 2019
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		0.100 1.000 14 2011 2018
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		0.100 1.000 12 2011 2018
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.100 0.818 11 2012 2015
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0239946
Disease: Fibrosis, Liver
Fibrosis, Liver 		0.100 1.000 11 2010 2019
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		0.080 0.875 8 2011 2017
dbSNP: rs12979860
rs12979860
IFNL4
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: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		0.050 1.000 5 2012 2015
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.050 1.000 5 2011 2017
dbSNP: rs12979860
rs12979860
IFNL4
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
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019158
Disease: Hepatitis
Hepatitis 		0.040 0.750 4 2011 2017
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections 		0.040 0.750 4 2014 2019
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		0.040 1.000 4 2013 2019
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0011226
Disease: Hepatitis D Infection
Hepatitis D Infection 		0.030 1.000 3 2014 2017
dbSNP: rs12979860
rs12979860
IFNL4
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 		0.030 1.000 3 2011 2017
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0011847
Disease: Diabetes
Diabetes 		0.030 1.000 3 2013 2015
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		0.030 1.000 3 2011 2017
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0019189
Disease: Hepatitis, Chronic
Hepatitis, Chronic 		0.030 1.000 3 2016 2018
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.030 1.000 3 2013 2015
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C4505456
Disease: HIV Coinfection
HIV Coinfection 		0.030 1.000 3 2013 2014
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis 		0.020 1.000 2 2012 2015
dbSNP: rs12979860
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		0.020 1.000 2 2013 2016