rs6478106, None

N. diseases: 2
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 0.820 1.000 3 2005 2019
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 0.700 1.000 1 2012 2012