Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs207016 1.000 0.040 21 17270927 intergenic variant G/A snv 1.00 1
rs26318 0.925 0.040 5 116352208 intron variant C/T snv 0.99 3
rs3759914 1.000 0.040 15 92393214 upstream gene variant C/T snv 0.97 1
rs324899 0.925 0.040 5 88619764 intron variant A/G snv 0.97 2
rs3759916 1.000 0.040 15 92392939 upstream gene variant C/T snv 0.97 1
rs3864075 1.000 0.040 3 7659884 intron variant G/A snv 0.96 1
rs10747050 1.000 0.040 9 137161424 splice region variant G/A snv 0.94 0.95 1
rs643410 1.000 0.040 9 109037283 intron variant A/C snv 0.93 1
rs133047 1.000 0.040 22 40631815 intron variant T/C snv 0.93 3
rs7752195 1.000 0.040 6 25418866 intron variant T/C snv 0.93 2
rs7732249 1.000 0.040 5 60070442 intron variant C/T snv 0.92 1
rs2104425 0.925 0.040 6 40277470 upstream gene variant T/C snv 0.91 4
rs10750489
NTM
1.000 0.040 11 131786445 intron variant C/G;T snv 0.91 1
rs227932 1.000 0.040 7 23584856 downstream gene variant A/G snv 0.90 1
rs1490191 1.000 0.040 1 151944275 upstream gene variant C/A snv 0.90 2
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs1521470 0.925 0.040 7 45607253 intron variant A/G snv 0.89 2
rs760816 1.000 0.040 1 4796871 downstream gene variant A/G snv 0.87 1
rs2486001 1.000 0.040 1 44010315 non coding transcript exon variant T/C snv 0.87 1
rs2255349 1.000 0.040 9 88201419 intergenic variant A/G snv 0.87 1
rs2710322 1.000 0.040 3 52783577 intron variant T/C snv 0.87 1
rs2440390 1.000 0.040 11 113416156 intron variant T/C snv 0.87 1
rs2518823 1.000 0.040 22 19972665 intron variant T/C snv 0.86 1
rs1355095 1.000 0.040 5 131913076 intron variant C/T snv 0.86 1
rs2962250 1.000 0.040 5 51094157 intergenic variant G/A snv 0.86 1