Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs1037189404
MUC1
0.776 0.280 1 155187519 missense variant C/T snv 8
rs766333007
MUC1
0.776 0.280 1 155192274 missense variant C/T snv 7.0E-06 8
rs372883
BACH1
0.827 0.360 21 29345416 3 prime UTR variant T/C snv 0.53 5
rs762581936
MUC4
0.827 0.240 3 195788569 missense variant C/G;T snv 1.1E-05; 1.1E-05 5
rs757797666
GATA6
0.925 0.240 18 22171617 missense variant G/T snv 1.4E-05 3
rs757238433
ISG20
0.882 0.200 15 88655497 missense variant G/A snv 1.2E-05 7.0E-06 3
rs1399364791
PMEL ; CDK2
0.882 0.240 12 55967046 missense variant G/A snv 4.0E-06 3
rs61732239
ADA
1.000 0.120 20 44625622 missense variant C/G;T snv 1.0E-03 2
rs4503083
IDO2
0.925 0.120 8 40015416 stop gained T/A snv 0.23 0.19 2
rs370640837
ABCA12
1.000 0.120 2 215019657 missense variant G/A;T snv 1.8E-04 1
rs1187237313
ABCB5
1.000 0.120 7 20727052 missense variant G/A snv 7.0E-06 1
rs757430763
ABLIM2
1.000 0.120 4 8061051 missense variant C/T snv 4.4E-05 1
rs200567888
EPHA3
1.000 0.120 3 89210327 missense variant G/T snv 1.2E-03 9.8E-04 1
rs10109853
IDO2
1.000 0.120 8 40005362 missense variant C/T snv 0.48 0.46 1
rs772906202
SYDE1
1.000 0.120 19 15110668 missense variant G/A snv 3.1E-05 7.0E-06 1