Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 4
rs2082412 0.925 0.120 5 159290781 downstream gene variant G/A snv 0.27 2
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98