Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10023113
CAMK2D
1.000 0.080 4 113625548 intron variant A/G snv 0.18 1
rs10429489 0.925 0.080 9 21787522 intergenic variant G/A snv 0.26 2
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 2
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 2
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 1
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 1
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 1
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 1
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 1
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 1
rs1057519858
STK11
1.000 0.080 19 1220495 missense variant G/T snv 1
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs1057523347
TP53
0.925 0.160 17 7673789 stop gained A/G;T snv 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs1077424
DAB1
1.000 0.080 1 57344632 intron variant G/C snv 0.52 1
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
rs11080466
PIEZO2
1.000 0.080 18 10899030 intron variant A/G snv 0.31 1
rs11207010
DAB1
1.000 0.080 1 57337214 intron variant G/C snv 0.41 1
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 9
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs11375254
TP63
0.882 0.080 3 189625454 intergenic variant A/-;AA;AAA;AAAA delins 3