Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2118181 0.851 0.040 15 48623687 intron variant T/C snv 0.23 6
rs1036477 0.882 0.040 15 48622729 intron variant A/G snv 0.24 5
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs919433 0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs7866503 0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs4774517 0.882 0.040 15 48467094 intron variant G/T snv 0.34 3
rs595244 0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs11635140 1.000 0.040 15 48490366 intron variant T/A;C snv 2
rs2247876 1.000 0.040 15 48639254 intron variant T/A;C snv 2
rs6493333 0.925 0.040 15 48646849 intron variant T/A;C snv 2
rs16960886 1.000 0.040 15 48407289 downstream gene variant G/A snv 0.11 1
rs2099562 1.000 0.040 15 48659080 downstream gene variant A/G snv 0.67 1
rs7173026 1.000 0.040 15 48659353 downstream gene variant C/T snv 0.75 1
rs7173410 1.000 0.040 15 48659577 downstream gene variant C/A;T snv 1
rs10851469 1.000 0.040 15 48676216 intergenic variant C/T snv 0.68 1
rs10851470 1.000 0.040 15 48678083 intergenic variant G/A snv 0.69 1
rs12442299 1.000 0.040 15 48672170 regulatory region variant G/A snv 0.66 1
rs12907144 1.000 0.040 15 48692625 intergenic variant A/G;T snv 1
rs12910178 1.000 0.040 15 48696754 regulatory region variant C/T snv 0.70 1
rs1506523 1.000 0.040 15 48675135 regulatory region variant G/A;C snv 1
rs1566816 1.000 0.040 15 48673021 intergenic variant C/T snv 0.74 1
rs2043682 1.000 0.040 15 48665546 upstream gene variant C/A snv 0.66 1
rs2045889 1.000 0.040 15 48692249 intergenic variant T/A snv 0.81 1
rs2045891 1.000 0.040 15 48695522 regulatory region variant C/A;T snv 1
rs2126905 1.000 0.040 15 48695847 regulatory region variant C/T snv 0.81 1