Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10163267 1.000 0.120 16 83940313 intron variant G/A;C snv 1
rs1016343 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10411210 0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1048369 0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4
rs10496040 1.000 0.120 2 55080510 5 prime UTR variant C/A snv 9.1E-02 1
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057520001 0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1059449 1.000 0.120 6 29942921 missense variant G/A snv 6.1E-02 9.0E-02 1
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs10795668 0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs10821936 0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7
rs10898880 0.925 0.160 11 72814066 upstream gene variant C/A snv 0.50 3
rs10934853 0.882 0.160 3 128319530 intron variant C/A snv 0.43 3
rs10993994 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs11081899 0.851 0.160 18 35344446 5 prime UTR variant G/A;C;T snv 4
rs11083846 0.882 0.200 19 46704397 splice region variant G/A snv 0.17 0.16 3
rs11155133 0.925 0.200 6 140848688 intron variant A/G snv 8.5E-02 2
rs11158728 1.000 0.120 14 68295488 intron variant G/A;C;T snv 1
rs11169571 0.851 0.200 12 50819982 3 prime UTR variant T/C snv 0.36 4