Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 7
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 7
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 3
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 3
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 2
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 2
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1
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
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
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
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
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