Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2069840
IL6 ; IL6-AS1
0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs3027898
IRAK1
0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs2280883
FOXP3
0.827 0.280 X 49252667 intron variant T/C snv 0.30 9
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs1234314
TNFSF4
0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7