Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs601338 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 1
rs8049439 0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 2
rs516246 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 1
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs1142287 1.000 0.040 1 155260340 synonymous variant C/T snv 0.34 0.36 1
rs7539625 1.000 0.040 1 67207082 intron variant G/A snv 0.33 0.30 1
rs11230563 0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31 1
rs1050152 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs6446272 1.000 0.040 3 49425854 intron variant G/A snv 0.28 0.30 1
rs3764147 0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs2108622 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 2
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs2298428 0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 5
rs2297909 0.925 0.080 1 200991179 intron variant G/A snv 0.27 0.27 2
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 1
rs9858542
BSN
0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 2
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs2024092 0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 1
rs2076753 1.000 0.040 16 50699463 intron variant G/A;T snv 0.20 1
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs2066843 0.925 0.040 16 50711288 synonymous variant C/A;T snv 0.19 1