Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003643 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 1
rs1003644 1.000 0.080 22 39280739 downstream gene variant G/A snv 0.31 1
rs1005999 1.000 0.080 2 104907333 intron variant C/T snv 0.25 1
rs1008591 1.000 0.080 19 46227357 upstream gene variant A/G snv 0.45 1
rs1019212 1.000 0.080 19 46225962 upstream gene variant G/A snv 0.45 1
rs10607450 1.000 0.080 11 118812058 regulatory region variant T/C snv 0.19 1
rs10892294 1.000 0.080 11 118796648 downstream gene variant G/C snv 0.19 1
rs111413387 1.000 0.080 17 46267043 non coding transcript exon variant A/C snv 0.14 1
rs1158810 1.000 0.080 9 119047241 intergenic variant T/C snv 0.50 1
rs11604811 1.000 0.080 11 72678939 upstream gene variant G/A;T snv 1
rs11655972 1.000 0.080 17 39250819 downstream gene variant C/T snv 0.78 1
rs11724614 1.000 0.080 4 102629091 downstream gene variant A/G snv 0.55 1
rs12103884 1.000 0.080 17 39889472 intergenic variant C/T snv 0.45 1
rs12358982 1.000 0.080 10 104094571 regulatory region variant A/G snv 0.14 1
rs12437560 1.000 0.080 15 61832507 upstream gene variant T/G snv 0.20 1
rs12694574 1.000 0.080 2 222129014 intergenic variant T/C snv 0.16 1
rs12712133 1.000 0.080 2 102249813 downstream gene variant A/G snv 0.57 1
rs12939565 1.000 0.080 17 39882136 downstream gene variant A/T snv 0.41 1
rs12941333 1.000 0.080 17 39884281 intergenic variant C/T snv 0.39 1
rs12950209 1.000 0.080 17 39892849 intergenic variant T/C snv 0.45 1
rs13097965 1.000 0.080 3 184621969 intergenic variant C/T snv 0.43 1
rs13098099 1.000 0.080 3 184621879 intergenic variant G/A snv 0.43 1
rs137603 1.000 0.080 22 39298220 downstream gene variant A/C snv 0.50 1
rs16863422 1.000 0.080 2 222125296 intergenic variant A/G snv 0.20 1
rs16977002 1.000 0.080 17 71919192 intergenic variant T/C snv 0.33 1