Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 10
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 10
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs9277952 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 4
rs1195571 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 3
rs180082 0.882 0.080 17 69955727 intergenic variant C/G;T snv 3
rs2116260 1.000 0.080 6 33057663 TF binding site variant T/C snv 8.6E-02 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs9931702
AKTIP
0.851 0.160 16 53492639 non coding transcript exon variant C/T snv 0.55 4
rs9302648
AKTIP
0.882 0.080 16 53493869 non coding transcript exon variant G/T snv 0.54 3
rs864622584
APC
1.000 0.080 5 112838623 missense variant G/A snv 1
rs997271472
APC
1.000 0.080 5 112838434 missense variant G/A;T snv 4.0E-06 1
rs5757465
APOBEC3G
0.882 0.080 22 39081118 synonymous variant T/C snv 0.37 0.31 3
rs807183
ATG4A
0.851 0.120 X 108094263 intron variant G/A snv 0.51 4
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs3744935
BCL2
0.882 0.080 18 63127447 3 prime UTR variant C/T snv 6.0E-03 3
rs799917
BRCA1
0.708 0.320 17 43092919 missense variant G/A;C;T snv 0.40; 1.6E-05 18
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15 13
rs4986764
BRIP1
0.827 0.120 17 61685986 missense variant A/G snv 0.60 0.61 8
rs7213430
BRIP1
0.851 0.080 17 61682813 3 prime UTR variant G/A snv 0.61 6
rs2048718
BRIP1
0.827 0.120 17 61863458 5 prime UTR variant C/T snv 0.42 5
rs11079454
BRIP1
0.882 0.080 17 61679808 3 prime UTR variant T/A;C snv 3