Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1444068378
FHL2
1.000 0.040 2 105363404 missense variant G/A snv 4.0E-06 1
rs104894421
LIG4
0.882 0.200 13 108210436 missense variant C/A;T snv 1.2E-05 4
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs115658307
APC
1.000 0.040 5 112707537 5 prime UTR variant C/T snv 4.8E-03 1
rs138386816
APC
1.000 0.040 5 112707566 5 prime UTR variant C/T snv 7.2E-03 1
rs75612255
APC
1.000 0.040 5 112737543 intron variant T/C snv 1
rs113017087
APC
1.000 0.040 5 112737780 intron variant T/C snv 5.4E-03 1
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs201820837
ETV6
0.925 0.040 12 11869532 missense variant G/A;T snv 2.4E-05; 6.4E-05 2
rs387906666
CBL
0.827 0.080 11 119278182 missense variant A/C;G snv 5
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs387906517
ABL1
0.827 0.120 9 130862919 missense variant G/A snv 6
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25