Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs989902
PTPN13
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53 12
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs9350
EXO1
0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs876659477
TP53
0.882 0.040 17 7673730 missense variant T/C snv 3
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 10
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104