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: rs2072907
rs2072907 		0.882 0.120 22 43936773 intron variant C/G snv 0.20
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.030 0.667 3 2008 2009
dbSNP: rs2896019
rs2896019 		0.790 0.160 22 43937814 intron variant T/G snv 0.20
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.810 1.000 3 2013 2018
dbSNP: rs12483959
rs12483959 		1.000 22 43930116 intron variant G/A;C;T snv
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 2 2011 2019
dbSNP: rs12483959
rs12483959 		1.000 22 43930116 intron variant G/A;C;T snv
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 2 2011 2019
dbSNP: rs2073082
rs2073082 		1.000 0.040 22 43964127 intron variant G/A snv 0.18
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.700 1.000 2 2012 2013
dbSNP: rs2896019
rs2896019 		0.790 0.160 22 43937814 intron variant T/G snv 0.20
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		Digestive System Diseases 0.710 1.000 2 2012 2018
dbSNP: rs2896019
rs2896019 		0.790 0.160 22 43937814 intron variant T/G snv 0.20
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
Nonalcoholic Steatohepatitis 		Digestive System Diseases 0.710 1.000 2 2014 2018
dbSNP: rs2896019
rs2896019 		0.790 0.160 22 43937814 intron variant T/G snv 0.20
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.710 1.000 2 2013 2014
dbSNP: rs3810622
rs3810622 		1.000 0.040 22 43942254 intron variant T/C;G snv 0.40
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.710 1.000 2 2013 2016
dbSNP: rs738491
rs738491 		0.882 0.040 22 43958231 intron variant C/T snv 0.34
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.710 1.000 2 2013 2015
dbSNP: rs738491
rs738491 		0.882 0.040 22 43958231 intron variant C/T snv 0.34
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.800 1.000 2 2013 2018
dbSNP: rs1010022
rs1010022 		1.000 22 43940430 intron variant A/G snv 0.20
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.700 1.000 1 2013 2013
dbSNP: rs1010023
rs1010023 		0.851 0.080 22 43940218 intron variant T/C snv 0.20
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs1010023
rs1010023 		0.851 0.080 22 43940218 intron variant T/C snv 0.20
CUI: C0015695
Disease: Fatty Liver
Fatty Liver 		Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1010023
rs1010023 		0.851 0.080 22 43940218 intron variant T/C snv 0.20
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.700 1.000 1 2013 2013
dbSNP: rs1010023
rs1010023 		0.851 0.080 22 43940218 intron variant T/C snv 0.20
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11090617
rs11090617 		1.000 22 43930820 intron variant C/T snv 0.18
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.700 1.000 1 2013 2013
dbSNP: rs12483959
rs12483959 		1.000 22 43930116 intron variant G/A;C;T snv
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.700 1.000 1 2013 2013
dbSNP: rs12483959
rs12483959 		1.000 22 43930116 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2011 2011
dbSNP: rs12484795
rs12484795 		22 43947746 intron variant A/C snv 0.21
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs12484809
rs12484809 		22 43929751 intron variant C/T snv 0.18
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs12485100
rs12485100 		22 43929636 intron variant G/A;T snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs1474745
rs1474745 		1.000 22 43953356 intron variant T/C snv 0.19
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.700 1.000 1 2013 2013
dbSNP: rs1883349
rs1883349 		1.000 22 43936063 intron variant G/A snv 0.19
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.700 1.000 1 2013 2013
dbSNP: rs1883350
rs1883350 		1.000 22 43932163 intron variant T/C snv 0.35
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.700 1.000 1 2013 2013