Source: GWASDB

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: rs12722489
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.850 1.000 2 2007 2018
dbSNP: rs12722489
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2010 2010