Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 8
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 11
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 11
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 7
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519937
PIK3CA
0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 7
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20