Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;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
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 11
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 11
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 11
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 10
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 10
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 10
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 9
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 8
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 8
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 8
rs398123316
PTEN
0.851 0.160 10 87925530 missense variant A/G;T snv 8
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 8