Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140516819
EGFR
7 55172999 missense variant A/C;G snv 4.0E-05 2.4E-04 4
rs1441008398
APC
5 112839334 missense variant C/T snv 4.0E-06 4
rs35918369
EGFR
7 55205613 missense variant C/T snv 3.1E-04 3.3E-04 4
rs876660427
APC
5 112838608 missense variant C/T snv 4
rs1219568637
EGFR
7 55143404 missense variant G/A snv 7.0E-06 2
rs1288422703
APC
5 112767386 missense variant G/A snv 4.0E-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
rs6964824
PRKAG2
7 151654146 intron variant T/C snv 0.31 2
rs772468040
FLT3
13 28057413 missense variant C/G;T snv 1.2E-05; 4.0E-06 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
rs587780053
PMS2
7 5977698 missense variant C/T snv 8.0E-06 1.4E-05 1
rs730881913
PMS2
7 6004023 missense variant C/T snv 4.0E-06 1
rs779512948
PMS2
7 5989800 missense variant C/G;T snv 4.0E-06 1
rs864622553
PMS2
7 5987540 missense variant C/G snv 1.2E-05 1.4E-05 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
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
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97