Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 5
rs2280141
PLEKHA1
1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 4
rs2249937
LOC112267968
1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 3
rs6726160
NONOP2
1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 3
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs3890745
MMEL1
0.925 0.200 1 2622185 intron variant T/C snv 0.40 4
rs1953126
PHF19
1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs11043097
LINC02752
11 11114248 intron variant T/C snv 0.15 2
rs1194849
SPRED2
2 65379519 intron variant T/C snv 0.49 2
rs4374642
KIAA1109
4 122179956 intron variant T/C snv 0.13 2
rs4626515 7 140204330 intergenic variant T/C snv 0.22 2
rs9295089
LOC105378083 ; TAGAP
6 159042932 non coding transcript exon variant T/C snv 0.20 2
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 16