rs2843403, MMEL1

N. diseases: 3
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.882 0.200 1 2597658 intron variant T/C snv 0.54 0.800 1.000 1 2012 2012
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.882 0.200 1 2597658 intron variant T/C snv 0.54 0.010 1.000 1 2017 2017
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.882 0.200 1 2597658 intron variant T/C snv 0.54 0.010 1.000 1 2017 2017