Disease: Multiple Sclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 7
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 6
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 5
rs926070
TSBP1-AS1 ; TSBP1
0.827 0.320 6 32289789 intron variant G/A snv 0.68 5
rs2777899
VMP1
0.851 0.160 17 59755030 intron variant T/A;G snv 4
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs1292034
RPS6KB1
0.882 0.160 17 59912499 intron variant G/A snv 0.56 3