Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10009145 1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34 1
rs1799913 0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs3027172 0.925 0.080 17 8152405 missense variant A/G snv 0.38 0.17 2
rs1443547 1.000 0.080 11 20601429 missense variant G/A snv 0.37 0.38 1
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1693482 0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1806201 0.776 0.200 12 13564574 synonymous variant G/A snv 0.32 0.24 8
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs595961 0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs2241894 1.000 0.080 4 99344976 synonymous variant T/A;C snv 4.0E-06; 0.30 3
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs6691840 0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs7165988 1.000 0.080 15 38696614 non coding transcript exon variant C/G;T snv 0.26; 4.0E-06 1
rs7171233 1.000 0.080 15 38696559 intron variant T/A snv 0.26 0.26 1
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs752949 0.925 0.160 11 35306201 synonymous variant C/T snv 0.23 0.22 3
rs878081 0.882 0.200 21 44288394 synonymous variant C/T snv 0.21 0.19 3
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs29230 0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 6