Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 1
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 1
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 1
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 2
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 2
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 1
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 4
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 3
rs1867277
PTCSC2 ; FOXE1
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 1
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54 1
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 1
rs2230641
CCNH
0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 1
rs4915076
VAV3
0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 3
rs11175834
LINC02454 ; LOC100507065
0.925 0.080 12 65598856 intron variant C/T snv 0.14 2