Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 12
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 11
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 8
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 6
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs121913386
CDKN2A
0.807 0.120 9 21971018 missense variant G/A;T snv 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs121913535
KRAS
0.742 0.320 12 25245348 missense variant C/A;G;T snv 5
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 4
rs121913428
EGFR
0.827 0.120 7 55174015 missense variant G/A;C snv 4