Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 4
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 5
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs12722496
IL2RA
0.925 0.160 10 6054704 intron variant A/G snv 7.5E-02 2
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 3
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 6
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 4
rs2051549
HLA-DQB2
0.851 0.280 6 32762309 intron variant G/A snv 0.64 4
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2281808
SIRPG
0.925 0.160 20 1629905 intron variant T/A;C snv 4
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 8
rs241427
TAP2
0.925 0.160 6 32836637 intron variant A/G;T snv 2
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 6
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14