Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
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
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3