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
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
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
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs80358972
BRCA2
0.742 0.480 13 32356472 stop gained C/A;T snv 8.0E-06; 3.2E-05 12
rs746284240
MDM2
0.763 0.240 12 68809243 missense variant A/G snv 11
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv 9
rs1322648460
LOC100507144 ; CD44
0.776 0.320 11 35139332 frameshift variant G/- delins 9
rs1037189404
MUC1
0.776 0.280 1 155187519 missense variant C/T snv 8
rs121909235
PTEN
0.851 0.240 10 87957919 missense variant G/A snv 8
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs1064793929
TP53
0.882 0.280 17 7675167 frameshift variant A/-;AA delins 5
rs1430452530
HIF1A-AS3 ; HIF1A
0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 5
rs762581936
MUC4
0.827 0.240 3 195788569 missense variant C/G;T snv 1.1E-05; 1.1E-05 5
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 5
rs11125529
ACYP2
0.882 0.280 2 54248729 intron variant C/A;T snv 3
rs1399364791
PMEL ; CDK2
0.882 0.240 12 55967046 missense variant G/A snv 4.0E-06 3
rs151341424
STRA6
0.925 0.120 15 74190856 missense variant CC/TT mnv 3
rs757797666
GATA6
0.925 0.240 18 22171617 missense variant G/T snv 1.4E-05 3
rs1374154597
PPP2R3A
1.000 0.120 3 136023097 frameshift variant -/G delins 2
rs1569119395
WNT7B
0.925 0.120 22 45949926 stop gained G/A snv 2
rs191544901
MUC1
0.925 0.240 1 155187241 missense variant C/A;T snv 4.0E-06; 8.0E-06 2
rs397518481
RARB
0.925 0.120 3 25501230 stop gained C/G;T snv 2