Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs144848 0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs2180314 0.776 0.200 6 52752933 missense variant C/G snv 0.60 0.52 8
rs2240308 0.701 0.360 17 65558473 missense variant G/A snv 0.47 0.39 18
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25