Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2129035 1.000 0.040 8 109831384 intergenic variant C/A snv 0.38 1
rs2169650 1.000 0.040 11 67596446 intergenic variant A/G;T snv 1
rs2433752 1.000 0.040 12 114854163 intergenic variant A/G snv 0.13 1
rs2531815 1.000 0.040 6 28468283 intergenic variant C/T snv 0.44 1
rs2567446 1.000 0.040 15 95720753 intron variant A/G snv 0.62 1
rs2596551 1.000 0.040 6 31364462 upstream gene variant A/C snv 0.16 1
rs2743941 1.000 0.040 6 29787674 upstream gene variant T/C;G snv 1
rs2832616 1.000 0.040 21 30101474 downstream gene variant C/T snv 0.20 1
rs374644 1.000 0.040 1 225918985 intron variant G/T snv 1
rs656451 1.000 0.040 16 77039597 intergenic variant A/C;G snv 2.4E-03 1
rs6789378 1.000 0.040 3 162449608 intergenic variant G/A snv 0.67 1
rs68191 1.000 0.040 6 33512961 regulatory region variant T/C;G snv 1
rs6903982 1.000 0.040 6 27577965 intergenic variant T/C;G snv 1
rs6910968 1.000 0.040 6 27936403 upstream gene variant C/T snv 0.13 1
rs6911476 1.000 0.040 6 26612135 non coding transcript exon variant C/T snv 0.10 1
rs7250581 1.000 0.040 19 29573489 intergenic variant A/G snv 0.89 1
rs7278845 1.000 0.040 21 34265162 intron variant A/G snv 0.14 1
rs7356849 1.000 0.040 6 26396511 downstream gene variant T/C snv 0.29 1
rs7813186 1.000 0.040 8 109844252 intergenic variant A/G snv 0.52 1
rs7834319 1.000 0.040 8 109865933 intergenic variant G/A snv 0.25 1
rs8025174 1.000 0.040 15 101279548 upstream gene variant C/A;T snv 1
rs922971 1.000 0.040 8 109817880 intergenic variant G/C;T snv 1
rs9262560 1.000 0.040 6 31040849 intergenic variant C/A;T snv 1
rs9277937 1.000 0.040 6 33217117 downstream gene variant T/C snv 8.2E-02 1
rs9283880 1.000 0.040 6 27747464 intergenic variant A/C snv 0.34 1