Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 1
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 1
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 1
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 1
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 1
rs987525 0.807 0.160 8 128933908 intron variant C/A snv 0.31 1
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs4822983 0.925 0.080 22 28719078 intron variant C/T snv 0.33 1
rs2285947 0.807 0.120 7 21544470 intron variant G/A snv 0.44 1
rs7242481 0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35 1
rs4785204 1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 1
rs12210050 0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 1
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 1
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 1
rs2494938 0.752 0.240 6 40568389 intron variant G/A snv 0.51 1
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 1
rs1050631 0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30 1
rs17761864 1.000 0.040 17 2268343 intron variant C/A snv 0.28 1
rs2239612 1.000 0.040 3 187075454 intron variant G/A snv 0.17 1
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 1
rs2239815 0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44 1
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 2
rs1042602 0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 2
rs2847281 1.000 0.040 18 12821594 intron variant A/G snv 0.32 2
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 3