Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10892286
DDX6
11 118771376 intron variant A/C snv 0.17 2
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 3
rs4288027
KIAA1109
4 122262050 intron variant A/C;G snv 0.13 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 8
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 7
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 7
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 7
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 7
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs10491322
PPP2CA
0.925 0.120 5 134194449 3 prime UTR variant A/G snv 9.5E-02 3
rs11984075
ELMO1
7 37397251 intron variant A/G snv 0.14 2
rs1355208 2 30222456 intergenic variant A/G snv 0.65 2
rs2893008
IL21-AS1
4 122631659 intron variant A/G snv 5.1E-02 2
rs6706689
PUS10
2 60943910 intron variant A/G snv 0.48 2
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs1772408
IFI16
1 159035859 intron variant A/G;T snv 2
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10