Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11074956 0.925 0.160 16 11243864 downstream gene variant G/T snv 0.34 2
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 7
rs13017599
NONOP2
0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 3
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs151719
HLA-DMB
0.925 0.160 6 32936123 non coding transcript exon variant C/T snv 0.72 2
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 9
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 6
rs17421624
TNXB
0.925 0.160 6 32098400 intron variant T/C snv 0.25 2
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11