Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
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
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 8
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs868162712
TCF4
0.925 0.040 18 55279598 missense variant G/A snv 3
rs867657798
TCF4
0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G 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
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs80359183
BRCA2
0.882 0.120 13 32380096 stop gained T/A;C snv 4
rs80357796
BRCA1
0.752 0.240 17 43094464 frameshift variant T/- del 11
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs779707422
FGFR1
0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 12
rs777169839
PPARGC1A
4 23828453 missense variant T/C;G snv 2.4E-05 2