Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4775769 15 48647691 intron variant T/G snv 0.93 2
rs4775762 1.000 0.040 15 48451808 intron variant T/C snv 0.76 1
rs714290 1.000 0.040 15 48459132 intron variant C/G snv 0.69 1
rs2303500 1.000 0.040 15 48447077 intron variant A/G snv 0.67 1
rs2042747 1.000 0.040 15 48436437 intron variant C/T snv 0.66 1
rs2303502 1.000 0.040 15 48444487 intron variant A/T snv 0.66 1
rs16960901 1.000 0.040 15 48413009 intron variant T/C snv 0.65 1
rs1042078 1.000 0.040 15 48410676 3 prime UTR variant G/A snv 0.64 1
rs8041668 1.000 0.040 15 48543158 intron variant T/C snv 0.62 1
rs6493328 1.000 0.040 15 48527305 intron variant G/A snv 0.49 1
rs668842 15 48599768 intron variant C/T snv 0.48 1
rs682938 1.000 0.040 15 48572170 intron variant A/G snv 0.47 1
rs920184 1.000 0.040 15 48600742 intron variant C/T snv 0.40 1
rs2437946 1.000 0.040 15 48633805 intron variant G/A snv 0.40 1
rs9806163 1.000 0.040 15 48511642 intron variant T/C snv 0.37 1
rs2306352 1.000 0.040 15 48513440 intron variant G/A snv 0.37 1
rs140605 1.000 0.040 15 48497437 intron variant T/C snv 0.28 0.35 1
rs10519177 0.925 0.040 15 48464998 intron variant A/G snv 0.35 2
rs2448485 1.000 0.040 15 48567536 intron variant A/G snv 0.35 1
rs4774517 0.882 0.040 15 48467094 intron variant G/T snv 0.34 3
rs589668 1.000 0.040 15 48543738 intron variant C/T snv 0.33 1
rs7184016 1.000 0.040 15 48518302 intron variant G/T snv 0.33 1
rs9806323 1.000 0.040 15 48473818 intron variant T/A snv 0.31 1
rs1036477 0.882 0.040 15 48622729 intron variant A/G snv 0.24 5
rs1678983 1.000 0.040 15 48638448 intron variant T/C snv 0.24 1