Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1010980331
FLCN ; MPRIP
0.925 0.120 17 17215072 missense variant T/C snv 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1048798213
APC
1.000 0.120 5 112837872 missense variant C/G snv 1
rs104893751
OGG1
0.882 0.240 3 9750423 missense variant G/A;C snv 2.2E-03; 4.0E-06 5
rs104893824
VHL
0.776 0.320 3 10142181 missense variant T/A;C snv 8
rs104893829
VHL
0.882 0.240 3 10142088 missense variant C/T snv 2.0E-04 3.8E-04 4
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049334
CAV1
0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 6
rs1049380
ITPR2
0.827 0.120 12 26336611 3 prime UTR variant G/T snv 0.69 5
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1055259
GSTM3 ; GSTM5
1.000 0.120 1 109734239 3 prime UTR variant T/C snv 0.12 1
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1060502375
FLCN
0.882 0.120 17 17228023 missense variant G/T snv 4.0E-06 3
rs1064794272
VHL
0.807 0.240 3 10146566 missense variant C/A snv 6
rs10771279
ITPR2
0.925 0.120 12 26377610 intron variant T/A;C snv 0.40 2
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10936602
LRRIQ4
0.882 0.240 3 169818849 upstream gene variant T/C snv 0.26 3
rs11203289
SDHB
0.882 0.240 1 17054012 missense variant G/A;C snv 4.1E-06; 3.1E-03 3
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131690838
FLCN
0.925 0.120 17 17228135 frameshift variant C/- del 3
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691061
SDHB
0.827 0.280 1 17054017 start lost C/T snv 6
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490