Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1476330207
IRF3
19 49660781 frameshift variant G/- delins 4.1E-06 1
rs17876183
PON2
7 95434956 missense variant C/T snv 1.2E-02 1.4E-02 1
rs17876205 7 95403792 downstream gene variant C/G snv 1.4E-02 1
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 4
rs6585827
PLEKHA1
1.000 0.040 10 122406099 intron variant G/A snv 0.47 3
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 3
rs17026688
GADL1
1.000 0.040 3 30845325 intron variant C/T snv 9.3E-03 2
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 4
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 3
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs4648356
TTC34
1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs654690
LOC112267968
1.000 0.080 6 159093746 intron variant T/A;C snv 3
rs6726160
NONOP2
1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 3
rs715412 1.000 0.080 11 118813901 regulatory region variant G/A snv 0.17 3
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 3
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 7
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4
rs10491322
PPP2CA
0.925 0.120 5 134194449 3 prime UTR variant A/G snv 9.5E-02 3
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 10
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 7