Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2271338 0.827 0.080 4 61996533 intron variant G/A snv 0.26 5
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs17522122 0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 5
rs4261436 0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43 3
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
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
rs137852972 0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 10
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs58064122 0.882 0.160 17 44913334 missense variant G/A;C snv 3
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs1040177874 0.925 0.040 2 208239914 missense variant G/A snv 4.0E-06 2
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2378456
LPP
0.807 0.200 3 188885218 3 prime UTR variant C/G;T snv 6
rs7115578 0.882 0.040 11 96266936 intron variant G/A snv 0.37 3
rs2431689 0.882 0.040 5 160472115 intron variant G/A snv 0.17 3
rs3745601 0.882 0.120 19 10113872 missense variant G/A snv 0.16 0.13 3
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs6089953 0.882 0.080 20 63659655 intron variant A/G snv 0.82 3
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21