Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs1234315
TNFSF4
0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs11168268
VDR
0.925 0.120 12 47858029 intron variant G/A snv 0.57 2
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1562444
MTNR1B
0.925 0.120 11 92982683 3 prime UTR variant G/A snv 0.55 2
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs12150220
NLRP1
0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs10911363
SMG7 ; NCF2
0.925 0.120 1 183580622 intron variant G/T snv 0.30 2
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs4958847
IRGM
0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs204989
GPSM3
0.925 0.120 6 32194075 intron variant G/A snv 0.21 2
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 7