Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs3748067 0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19