Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 35
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 23
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 21
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 14
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 12
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 11
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 9
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 7
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 7
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 5
rs121913484
FGFR3
0.851 0.240 4 1804365 missense variant A/T snv 5
rs587779333
PMS2 ; AIMP2
0.851 0.200 7 6009019 start lost T/A;C;G snv 4.0E-06; 2.8E-05 5
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 4
rs121913245
MET
0.925 0.120 7 116783420 missense variant T/C snv 3
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv 3
rs267607906
MLH1
1.000 0.160 3 37050576 stop gained A/C;G;T snv 3