Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 25
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 16
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 11
rs768824654
MSH2
1.000 0.120 2 47403390 start lost A/G snv 7.0E-06 6
rs7987649
FLT1
0.925 0.080 13 28320278 intron variant A/G snv 0.35 4
rs876660427
APC
5 112838608 missense variant C/T snv 4
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 3
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
rs1219568637
EGFR
7 55143404 missense variant G/A snv 7.0E-06 2
rs412396 20 43657322 downstream gene variant C/G snv 0.77 2
rs4725431
PRKAG2
7 151776093 intron variant T/C snv 0.19 2
rs4771249
FLT1
13 28439277 intron variant G/A;C snv 2
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 2
rs6964824
PRKAG2
7 151654146 intron variant T/C snv 0.31 2
rs1064793236
PMS2
7 5986802 missense variant C/T snv 7.0E-06 1
rs1961177
CYP19A1
15 51332881 intron variant C/T snv 0.21 1
rs201744589
TP53
0.882 0.240 17 7673728 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614