Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1019221239
APC
0.925 0.120 5 112835093 stop gained T/A;C;G snv 4.0E-06 3
rs1019340046
TP53
0.882 0.080 17 7674225 missense variant C/T snv 5
rs1021662947
PALB2
16 23614039 stop gained G/A snv 1
rs1023534466
FBXO11 ; MSH6
2 47795984 frameshift variant TAAA/- delins 1
rs1025339570
ATM
11 108249045 stop gained G/A;T snv 7.0E-06 1
rs1028347439
BRIP1
17 61801267 stop gained G/A snv 1
rs104886456
FANCC
0.925 0.120 9 95172033 splice region variant T/A snv 2.9E-04 2.1E-04 3
rs104886457
AOPEP ; FANCC
0.882 0.240 9 95101742 stop gained G/A snv 5.2E-05 7.7E-05 4
rs104893825
VHL
1.000 0.120 3 10149819 missense variant G/T snv 2
rs104893826
VHL
0.882 0.200 3 10142038 missense variant G/A;C snv 4
rs104893830
VHL
0.925 0.160 3 10146561 missense variant G/C;T snv 3
rs104893831
VHL
0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 4
rs104894094
CDKN2A
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 12
rs104894095
CDKN2A
0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 6
rs104894097
CDKN2A
0.807 0.240 9 21974757 missense variant C/A;G;T snv 1.7E-05; 1.3E-05 8
rs104894098
CDKN2A
0.851 0.200 9 21970982 missense variant A/T snv 5
rs104894099
CDKN2A
0.851 0.200 9 21971183 missense variant A/C;T snv 4.6E-06 5
rs104894109
CDKN2A
0.925 0.120 9 21971192 missense variant C/A;T snv 3
rs104894259
MAP4K2 ; MEN1
1.000 0.120 11 64805078 missense variant A/G;T snv 2
rs104894261
MAP4K2 ; MEN1
1.000 0.120 11 64804588 stop gained G/A snv 2
rs104894263
MEN1
1.000 0.120 11 64809695 missense variant G/C snv 2
rs104894264
MEN1 ; MAP4K2
1.000 0.120 11 64805132 missense variant C/A;G;T snv 2
rs104894266
MEN1
1.000 0.120 11 64807557 stop gained G/A snv 2
rs104894267
MEN1 ; MAP4K2
1.000 0.120 11 64804789 stop gained G/A;T snv 7.0E-06 2
rs104894302
SDHD
0.851 0.200 11 112089002 missense variant A/G;T snv 4.0E-06 5