Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1329032366
PDLIM5
0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs4579555
RAD21
0.882 0.080 8 116867092 intron variant A/G snv 4
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs1451539938
CD82
0.925 0.080 11 44618361 missense variant A/G snv 4.1E-06 7.0E-06 3
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs1223118092
LOC100506142 ; RHOQ
2 46576601 missense variant A/G snv 1
rs138281457
GRAP2
22 39955861 missense variant A/G snv 4.0E-06 3.5E-05 1
rs4328905
HPSE
4 83322396 intron variant A/G snv 0.18 0.18 1
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs141613848
SLC9A3R1
0.925 0.080 17 74768481 missense variant A/T snv 1.0E-03 1.2E-03 4
rs1194624468
PTK2
1.000 0.040 8 140700895 missense variant A/T snv 1.6E-05 2
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs1431090090
ZEB1
1.000 0.040 10 31520347 missense variant C/A snv 4.0E-06 2
rs1383618437
ATAT1
6 30627473 missense variant C/A snv 4.0E-06 1
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs104894403
GJB2
0.851 0.240 13 20189386 missense variant C/A;G;T snv 4.0E-06 7
rs772092699
EPHB2
0.925 0.080 1 22912497 missense variant C/A;G;T snv 4.0E-06 3