Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs398124146
CREBBP
0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs747241612
FBXW7
0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs121913287
PIK3CA
0.752 0.400 3 179199088 missense variant G/A snv 12
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 13
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 15
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 15
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs121913283
PIK3CA
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16