Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 4
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 3
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs4915076
VAV3
0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 3
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs12990503
DIRC3
0.925 0.080 2 217429494 intron variant C/G snv 0.64 2
rs9400239
FOXO3
1.000 6 108656460 5 prime UTR variant T/C snv 0.55 2
rs11175834
LINC02454 ; LOC100507065
0.925 0.080 12 65598856 intron variant C/T snv 0.14 2
rs9858271
LOC105377110
0.925 0.080 3 59559604 intron variant G/A snv 0.80 2
rs1874564
LOC107986291 ; LOC105377294
0.925 0.080 4 76936952 intergenic variant G/A snv 0.58 2
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 2
rs6996585
NRG1
0.925 0.080 8 32543285 intron variant A/G snv 0.37 2
rs4649295
PCNX2
0.925 0.080 1 233280792 intron variant T/C snv 0.60 2
rs10808556
CASC8 ; POU5F1B ; PCAT1 ; CCAT2
0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50 1
rs2230641
CCNH
0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 1
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 1
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 1