Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 8
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 7
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs31563 0.851 0.160 5 135899917 intron variant C/A;T snv 5
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 5
rs12425791 0.882 0.120 12 674318 downstream gene variant G/A;C snv 4
rs12570088 0.851 0.160 10 58178575 intergenic variant A/G snv 4.1E-02 4
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 4
rs4968782 1.000 0.080 17 63471115 upstream gene variant G/A;T snv 4
rs541458 0.851 0.080 11 86077309 regulatory region variant C/T snv 0.71 4
rs6834555 0.882 0.200 4 10060702 regulatory region variant G/A snv 0.74 4
rs714873 0.882 0.200 4 10057994 upstream gene variant G/A snv 0.74 4
rs79721419 0.851 0.160 9 22200957 downstream gene variant G/A snv 7.4E-03 4
rs1544210 0.882 0.240 10 92728044 regulatory region variant G/A snv 0.39 3
rs157595 1.000 0.080 19 44922203 upstream gene variant A/G;T snv 3
rs1595014 0.882 0.120 7 12148903 intergenic variant T/A snv 0.23 3
rs4605275 1.000 0.080 19 44835236 intergenic variant T/C snv 0.69 3