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: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.900 1.000 3 2007 2019
dbSNP: rs12722489
rs12722489
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: rs3118470
rs3118470
0.752 0.360 10 6059750 intron variant T/A;C snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2011 2011
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011