Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 4
rs16860926 3 186609982 intron variant T/C snv 2.6E-02 4
rs2523575 6 31361049 upstream gene variant C/G snv 0.20 4
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs563290 2 21065354 intergenic variant G/A snv 0.69 4
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs585967 1.000 0.040 2 21047682 upstream gene variant A/C snv 0.81 4
rs754523 2 21088819 intergenic variant A/G snv 0.28 4
rs754524 2 21088669 intergenic variant T/G snv 0.19 4
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 4
rs10260606 7 44544952 upstream gene variant G/A;C snv 3
rs10788994 1 55035303 upstream gene variant C/T snv 0.20 3
rs11577931 1 109278262 downstream gene variant A/G snv 5.5E-02 3
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs1713222 2 21048451 upstream gene variant A/G snv 0.82 3