Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1075309 1.000 0.040 2 5113465 intergenic variant C/T snv 0.20 1
rs11031728 1.000 0.040 11 32342070 intron variant C/G snv 0.18 1
rs12437118 1.000 0.040 14 76517387 intron variant G/A;C snv 1
rs12456774 1.000 0.040 18 22592612 intergenic variant G/A snv 0.17 1
rs17175227 1.000 0.040 14 70035333 downstream gene variant G/A;C snv 2.1E-02 1
rs2057178 1.000 0.040 11 32342641 intron variant G/A snv 0.18 1
rs2202157 1.000 0.040 3 26501929 intergenic variant C/T snv 0.12 1
rs39509 1.000 0.040 8 89791937 downstream gene variant G/A snv 0.65 1
rs4859843 1.000 0.040 4 77439033 intron variant T/C;G snv 1
rs4859846 1.000 0.040 4 77439174 intron variant G/A snv 0.19 1
rs6676375 1.000 0.040 1 242711583 intergenic variant T/C snv 0.15 1
rs8087945 1.000 0.040 18 22596123 intergenic variant A/G snv 0.61 1
rs932347 1.000 0.040 1 209882285 intergenic variant C/T snv 0.15 1
rs958617 1.000 0.040 4 77684215 intergenic variant A/G snv 0.56 1
rs2542670 1.000 0.040 17 37294135 intron variant A/G;T snv 1
rs2115819 1.000 0.040 10 45405641 intron variant A/G snv 0.42 1
rs7111432 1.000 0.040 11 429659 splice region variant C/G;T snv 4.0E-06; 0.56 1
rs1017281 1.000 0.040 8 130234967 intron variant G/A snv 0.37 1
rs10956514 1.000 0.040 8 130240512 intron variant A/G snv 0.37 1
rs11774633 1.000 0.040 8 130177997 intron variant C/T snv 0.61 1
rs4236749 1.000 0.040 8 130052907 3 prime UTR variant C/T snv 0.16 1
rs4733781 1.000 0.040 8 130284521 intron variant A/C snv 0.29 1
rs1925714 1.000 0.040 1 228515588 upstream gene variant A/G snv 0.81 1
rs451390 1.000 0.040 21 41923401 intron variant G/C snv 7.5E-02 1
rs411089 1.000 0.040 1 158255035 intron variant C/T snv 0.39 0.43 1