Disease: Steatohepatitis ×
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: 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: rs738409
rs738409 		0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		Digestive System Diseases 0.100 0.944 89 2009 2020
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: rs2294918
rs2294918 		0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs738491
rs738491 		0.882 0.040 22 43958231 intron variant C/T snv 0.34
CUI: C2711227
Disease: Steatohepatitis
Steatohepatitis 		Digestive System Diseases 0.010 1.000 1 2015 2015