Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 34
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 16
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 13
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 10
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 9
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 7
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 7
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 7
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 7
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6