Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs774994509
SOD1
0.851 0.080 21 31667296 missense variant A/G snv 4.0E-06 5
rs1405999227
EGFR
0.925 0.160 7 55156637 missense variant A/G snv 4.0E-06 3
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs121908585
PDGFRA
0.827 0.080 4 54285926 missense variant A/T snv 9
rs28937900
FKRP
0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs391745 0.925 0.080 X 97839482 intergenic variant C/G;T snv 3
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
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
rs483352809
TUBB4A
0.882 0.120 19 6495754 missense variant C/T snv 5
rs877610
TRPV1
1.000 17 3572196 synonymous variant C/T snv 4.6E-02 7.5E-02 3
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs121912433
SOD1
0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7
rs6162
CYP17A1
0.925 0.080 10 102837224 synonymous variant G/A snv 0.42 0.40 3
rs61731956
NR1H3 ; MADD
0.925 0.080 11 47268596 missense variant G/A snv 2.2E-04 2.6E-04 3
rs1800876
CMA1
1.000 14 24510007 upstream gene variant G/A snv 0.24 2
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7