Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77581414 1.000 0.080 19 10823418 non coding transcript exon variant T/A;C snv 1
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 11
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs10861905 0.925 0.120 12 108373556 regulatory region variant C/A snv 7.6E-02 2
rs2278911 0.925 0.080 3 108579413 missense variant C/T snv 0.16 0.12 2
rs2273669 0.925 0.080 6 108963986 intron variant A/G snv 0.19 2
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs1046040 0.925 0.080 19 1095515 upstream gene variant G/A snv 0.21 2
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs75823044 1.000 0.080 13 109708437 intron variant C/T snv 7.6E-03 1
rs7483 0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs11102001 0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 4
rs7986346 0.925 0.080 13 109801260 intron variant G/A;C;T snv 2
rs3746165 0.925 0.080 19 1102212 upstream gene variant A/G snv 0.54 3
rs2301241
TXN
0.827 0.160 9 110257228 upstream gene variant G/A;T snv 5
rs2536 0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs11691517 1.000 0.080 2 111135519 intron variant T/G snv 0.22 1
rs56366063 1.000 0.080 2 111146954 intron variant C/A snv 7.2E-02 1
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs2788612 1.000 0.080 1 111873741 intron variant T/C snv 0.96 1
rs3806317 0.925 0.080 1 11188159 intron variant A/G snv 3.4E-02 2
rs1034528 0.882 0.120 1 11189075 intron variant G/C snv 0.30 5
rs14133 0.807 0.200 11 111911973 5 prime UTR variant G/C snv 0.27 7
rs17036508 0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02 4