Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2019960
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.800 1.000 3 2010 2014
dbSNP: rs2019960
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011