Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs3129720 0.851 0.280 6 32695854 intergenic variant T/C snv 0.76 4
rs926103
SH2D2A ; NTRK1
0.925 0.120 1 156815190 missense variant T/C snv 0.64 0.57 2