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: rs11810217
rs11810217
EVI5
1.000 0.080 1 92682820 intron variant C/T snv 0.20
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.810 1.000 1 2011 2017
dbSNP: rs10735781
rs10735781
EVI5
1.000 0.080 1 92655550 intron variant G/C snv 0.57
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.710 1.000 1 2011 2017