Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs10190751 0.882 0.120 2 201141373 splice acceptor variant G/A snv 0.18 0.26 4
rs2621416 0.882 0.280 6 32774091 intergenic variant T/C snv 0.26 4