Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs6013897 0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23 7
rs907580 0.851 0.080 9 97860315 downstream gene variant T/A;C;G snv 4
rs2145418 0.882 0.080 1 118422631 intergenic variant C/A snv 0.78 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs1064795638
BAP1
0.851 0.080 3 52403251 stop gained G/A snv 7
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs747463591
CCDC6
0.882 0.080 10 59906391 missense variant C/A;G;T snv 4.9E-06; 9.9E-06 3
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs778212685
CHEK2
0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs786203472
CHEK2
0.827 0.120 22 28719414 start lost T/C snv 5
rs863224748
CHEK2
0.827 0.120 22 28734721 start lost T/C snv 5
rs78929565
CLOCK
0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs1169803481
EGFR
0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 7
rs1032006770
EGFR
0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs2227869
ERCC5 ; BIVM-ERCC5
0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9