Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121909235
PTEN
0.851 0.240 10 87957919 missense variant G/A snv 8
rs1430452530
HIF1A-AS3 ; HIF1A
0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 5
rs1064793929
TP53
0.882 0.280 17 7675167 frameshift variant A/-;AA delins 5
rs1284110310
ERBB2
0.882 0.200 17 39706999 missense variant G/A snv 7.0E-06 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
rs10919791 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 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
rs2242241
DOK2
0.925 0.200 8 21909370 missense variant A/C snv 1.0E-02 7.9E-03 2
rs397518481
RARB
0.925 0.120 3 25501230 stop gained C/G;T snv 2
rs67437265
DCK
0.925 0.160 4 71022523 missense variant C/T snv 1.8E-02 2.3E-02 2
rs763861742
MUC1
0.925 0.240 1 155187268 missense variant C/G;T snv 1.2E-05 2
rs9854771
TP63
0.925 0.240 3 189790682 intron variant G/A snv 0.34 2
rs11845046
MIA2
1.000 0.120 14 39246997 missense variant A/G snv 0.22 0.20 2
rs1374154597
PPP2R3A
1.000 0.120 3 136023097 frameshift variant -/G delins 2
rs118203958
STRA6
1.000 0.120 15 74190889 missense variant G/A snv 4.0E-06 1.4E-05 1
rs118203959
STRA6
1.000 0.120 15 74180121 missense variant G/A snv 1.6E-05 1
rs118203960
STRA6
1.000 0.120 15 74180153 missense variant G/A snv 1.2E-05 3.5E-05 1
rs118203961
STRA6
1.000 0.120 15 74196145 missense variant G/A snv 1
rs118203962
STRA6
1.000 0.120 15 74189244 missense variant T/G snv 5.4E-04 4.1E-04 1