Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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 19
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 11
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 10
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 9
rs63750206
MLH1
0.807 0.200 3 36996701 missense variant G/A;C;T snv 7
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 5
rs201744589
TP53
0.882 0.240 17 7673728 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 3
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 3
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs1057519803
ERBB3
0.925 0.080 12 56088138 missense variant G/A snv 2
rs112431538
TP53
1.000 0.120 17 7673767 missense variant C/T snv 7.0E-06 2
rs17280262 14 96587587 upstream gene variant C/T snv 5.1E-02 1
rs4812219 20 60847915 intergenic variant C/T snv 0.13 1
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs587778966
MLH1
0.925 0.160 3 36996698 frameshift variant -/C delins 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1