Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
64 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.900 1.000 23 2009 2018
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
89 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.100 1.000 21 2010 2016
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
21 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.080 1.000 8 2011 2017
Liver diseases
CUI: C0023895
Disease: Liver diseases
26 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.050 1.000 5 2011 2015
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
31 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.040 1.000 4 2011 2014
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
192 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.030 0.667 3 2012 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
419 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.030 1.000 3 2013 2016
Fatty Liver
CUI: C0015695
Disease: Fatty Liver
24 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.020 1.000 2 2013 2014
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
41 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.020 1.000 2 2013 2014
Acute hepatitis C
CUI: C0400914
Disease: Acute hepatitis C
2 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2012 2012
Anemia
CUI: C0002871
Disease: Anemia
44 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2013 2013
Anemia, Hemolytic
CUI: C0002878
Disease: Anemia, Hemolytic
9 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2012 2012
Arthropathy
CUI: C0022408
Disease: Arthropathy
7 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2016 2016
Bleeding tendency
CUI: C1458140
Disease: Bleeding tendency
5 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2017 2017
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
17 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2017 2017
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
22 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2012 2012
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
48 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2014 2014
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
32 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2014 2014
Congenital Bleeding Disorder
CUI: C3641106
Disease: Congenital Bleeding Disorder
2 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2017 2017
Congenital hypoplasia of adrenal gland
15 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2012 2012
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
219 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2013 2013
Hemophilia, NOS
CUI: C0684275
Disease: Hemophilia, NOS
4 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2013 2013
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
209 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2012 2012
Hepatitis D Infection
CUI: C0011226
Disease: Hepatitis D Infection
3 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 0.010 1.000 1 2014 2014