Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 4
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2
rs7172677 0.925 0.080 15 75132252 intergenic variant A/C snv 0.71 2
rs1857066
LOC100506023 ; TNFSF4
1.000 0.040 1 173363490 non coding transcript exon variant A/C snv 0.79 1
rs12531711
TNPO3
0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 3
rs3130573
PSORS1C2 ; PSORS1C1
1.000 0.040 6 31138491 non coding transcript exon variant A/C;G snv 8.1E-06; 0.33 1
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs2834167
IL10RB
0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 11
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs275653
AGTR1
0.882 0.120 3 148697758 upstream gene variant A/G snv 0.20 5