Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2853495
ND5 ; ND4
1.000 0.040 MT 11719 synonymous variant G/A snv 1
rs2232365
FOXP3
0.716 0.480 X 49259429 intron variant T/C snv 16
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs2294021
CCDC22
0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs1801198
TCN2
0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 9
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 7
rs9606756
TCN2
0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 7
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs140135
ZMAT5 ; UQCR10
0.827 0.120 22 29767846 non coding transcript exon variant C/G snv 0.79 5
rs5757584 0.827 0.120 22 39266545 intron variant C/G;T snv 5
rs142430606
IL17REL
0.925 0.040 22 49998059 missense variant G/A;T snv 1.1E-02; 4.4E-06 3
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 3
rs35873774
XBP1
0.925 0.040 22 28795944 intron variant A/G snv 4.6E-02 3
rs5763767
HORMAD2
0.925 0.040 22 30097893 intron variant G/A;T snv 3
rs200958270
IL17REL
1.000 0.040 22 49999850 missense variant T/C snv 1.1E-02 6.1E-03 2
rs5771069
IL17REL
0.925 0.120 22 49997051 missense variant A/G snv 0.56 0.55 2
rs138788
TOM1 ; MIR3909
1.000 0.040 22 35333728 intron variant G/A snv 0.49 1
rs713669
IL17REL
1.000 0.040 22 50013342 upstream gene variant C/G;T snv 1
rs861857
YDJC
1.000 0.040 22 21628051 upstream gene variant C/G;T snv 0.51 1