Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 4
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
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 2
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs2546890
LOC285626
0.882 0.200 5 159332892 non coding transcript exon variant A/G snv 0.52 3
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5