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
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
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs1346044
WRN
0.708 0.440 8 31167138 missense variant T/C snv 0.24 0.23 23
rs172378 0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs2228479 0.763 0.280 16 89919532 missense variant G/A;C snv 7.8E-02; 4.0E-06 11
rs12711521 0.807 0.240 1 11030859 missense variant C/A snv 0.74 0.63 7
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs587781386 0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3
rs764562217 0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs8094402
MBP
0.882 0.120 18 76995493 intron variant A/G snv 0.25 3