Disease: Tumor Cell Invasion
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs1049074086
CTSD
0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 9
rs1056123575
ADAMTS1
0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs11662595
HRH4
0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs1172398253
CCN1
0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs1196644309
TXNIP
1.000 0.080 1 145995155 missense variant G/A snv 3
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121917887
NME1-NME2 ; NME1
0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13