Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
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
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs1024446168
SYN1 ; TIMP1
1.000 0.040 X 47583421 synonymous variant C/A snv 1.7E-05 1
rs4819554
IL17RA
0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 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
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
rs2283790
UBE2L3
0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs715572
TIMP3 ; SYN3
0.925 0.040 22 32838944 intron variant G/A snv 0.18 3
rs11547635
TIMP3 ; SYN3
1.000 0.040 22 32857305 synonymous variant C/A;T snv 0.11 1
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs2823288 0.827 0.120 21 15448569 intron variant G/A snv 0.22 5
rs4456788
GATD3A
0.827 0.120 21 44196441 intron variant G/A snv 5
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 4
rs7282490
GATD3A
0.882 0.080 21 44195858 intron variant G/A;T snv 4
rs2150414
BRWD1
1.000 0.040 21 39243062 intron variant A/G snv 0.52 1