Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 52
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
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs104894360
KRAS
0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14
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
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 11
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 10
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 8
rs121917902
ERCC6 ; PGBD3
0.790 0.440 10 49524073 stop gained G/A snv 7
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 7
rs387906660
BRAF
0.790 0.280 7 140801550 missense variant G/A;C;T snv 7
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 6
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs387906661
BRAF
0.807 0.280 7 140801551 missense variant T/G snv 6
rs397516895
BRAF
0.827 0.280 7 140753392 missense variant A/T snv 5
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 3
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 3