Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 28
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 12
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 12
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 8
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs3091307 0.925 0.160 5 132653444 intron variant A/G snv 0.34 5
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs7512552 1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs1295686 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs176095 0.925 0.160 6 32190542 upstream gene variant A/G snv 0.22 3
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 2
rs7127307 1.000 0.120 11 128317488 regulatory region variant T/C snv 0.47 2