Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs774265827
VEGFA
6 43780773 missense variant G/A;T snv 8.0E-06; 2.0E-05 1
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs771563543
ZEB1
0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs769696078
EGFR
0.925 0.040 7 55154128 missense variant G/A snv 3
rs766727892
TCF7L2
0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs762584624
MYL2
12 110919162 missense variant C/A snv 4.0E-06 1
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs757066045
CDKN2A
0.882 0.040 9 21974725 missense variant C/T snv 8.2E-06 4
rs754820004
CUL3
2 224557736 missense variant T/C snv 4.0E-06 1
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs745934102
PDPN
0.882 0.040 1 13607281 missense variant G/A snv 3.2E-05 1.4E-05 5
rs745564626
XRCC3 ; KLC1
0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs727503094
LRRC56 ; HRAS
0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs63749833
MLH1
3 36996639 missense variant G/T snv 1
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 15