Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1288422703
APC
5 112767386 missense variant G/A snv 4.0E-06 2
rs876660427
APC
5 112838608 missense variant C/T snv 4
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 11
rs1441008398
APC
5 112839334 missense variant C/T snv 4.0E-06 4
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs6964824
PRKAG2
7 151654146 intron variant T/C snv 0.31 2
rs4725431
PRKAG2
7 151776093 intron variant T/C snv 0.19 2
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs772468040
FLT3
13 28057413 missense variant C/G;T snv 1.2E-05; 4.0E-06 2
rs7987649
FLT1
0.925 0.080 13 28320278 intron variant A/G snv 0.35 4
rs4771249
FLT1
13 28439277 intron variant G/A;C snv 2
rs587778966
MLH1
0.925 0.160 3 36996698 frameshift variant -/C delins 3
rs63750206
MLH1
0.807 0.200 3 36996701 missense variant G/A;C;T snv 9
rs412396 20 43657322 downstream gene variant C/G snv 0.77 2
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs768824654
MSH2
1.000 0.120 2 47403390 start lost A/G snv 7.0E-06 6
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18