Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs1057519771
ABL1
1.000 0.080 9 130872201 missense variant G/C snv 2
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs200863613
CDKN2A
0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs438034
CENPF
0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs10009228
CHRNA9
4 40354405 missense variant A/G snv 0.78 0.76 1
rs104893626
CXCR4 ; LOC112268426
0.827 0.280 2 136114915 stop gained G/C snv 11
rs2073778
DGCR8
22 20087052 non coding transcript exon variant C/T snv 0.12 1
rs720012
DGCR8
22 20111059 3 prime UTR variant G/A snv 0.12 1
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
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
rs2227983
EGFR
0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs961150162
EGFR
7 55198779 missense variant G/A;C snv 3
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs557263543
FGFR1
8 38412508 3 prime UTR variant C/T snv 3
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs7121
GNAS
0.882 0.160 20 58903752 missense variant C/G;T snv 0.54 6