rs2019960, PVT1

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.
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.925 0.160 8 128180025 intron variant T/C snv 0.27 0.800 1.000 3 2010 2014
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.925 0.160 8 128180025 intron variant T/C snv 0.27 0.800 1.000 1 2011 2011