Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs2296147
BIVM-ERCC5 ; ERCC5
0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs121908585
PDGFRA
0.827 0.080 4 54285926 missense variant A/T snv 9
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs121912456
SOD1 ; LOC102724449
0.851 0.120 21 31659806 missense variant G/C snv 6
rs483352809
TUBB4A
0.882 0.120 19 6495754 missense variant C/T snv 5
rs1062577
ESR1
0.882 0.080 6 152102770 3 prime UTR variant T/A;G snv 4
rs391745 0.925 0.080 X 97839482 intergenic variant C/G;T snv 3
rs1800876
CMA1
1.000 14 24510007 upstream gene variant G/A snv 0.24 2
rs7201637
HSD17B2
1.000 16 82081670 intron variant T/A snv 9.0E-02 2
rs121912433
SOD1
0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs774994509
SOD1
0.851 0.080 21 31667296 missense variant A/G snv 4.0E-06 5
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101