rs16851720, RNF7

N. diseases: 5
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.
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.827 0.120 3 141744456 intron variant A/C snv 0.21 0.810 0.500 2 2012 2017
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.827 0.120 3 141744456 intron variant A/C snv 0.21 0.010 1 2017 2017
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.827 0.120 3 141744456 intron variant A/C snv 0.21 0.010 1 2017 2017
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.827 0.120 3 141744456 intron variant A/C snv 0.21 0.700 1.000 1 2012 2012
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.827 0.120 3 141744456 intron variant A/C snv 0.21 0.010 1.000 1 2017 2017