Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs55743914
PTPRK
0.882 0.160 6 127972417 intron variant C/T snv 0.18 3
rs72975916
PTPRK
1.000 0.080 6 127972910 intron variant C/T snv 0.12 1
rs9491896
PTPRK
1.000 0.080 6 127979804 intron variant G/A snv 8.5E-02 1
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11875687
PTPN2
1.000 0.080 18 12843138 intron variant T/C snv 0.17 1
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs61907765
MIR6090 ; ETS1
1.000 0.080 11 128522042 5 prime UTR variant C/G;T snv 0.17 0.15 1
rs4128561
ETS1
1.000 0.080 11 128545234 intron variant T/C snv 0.58 1
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs80209296
PTPN2
0.925 0.200 18 12860802 intron variant G/A snv 2
rs5979785 0.925 0.160 X 12953405 intergenic variant C/T snv 2
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs77027760 1.000 0.080 6 137680924 intron variant G/A snv 0.15 1
rs17264332 0.925 0.200 6 137684378 intron variant A/G;T snv 2
rs4956400 1.000 0.080 4 141556189 intergenic variant T/C snv 0.75 1
rs11100722 1.000 0.080 4 141616307 intergenic variant G/C snv 0.77 1
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8