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
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs3177928
HLA-DRA
0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 8
rs3761959
FCRL3
0.827 0.320 1 157699488 intron variant C/A;G;T snv 7