Source: BEFREE ×
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-06 484
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 23
rs1805010
IL4R
0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 11
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 6
rs1049380
ITPR2
0.827 0.120 12 26336611 3 prime UTR variant G/T snv 0.69 5
rs7105934
LOC102724265
0.827 0.120 11 69424973 upstream gene variant G/A;C snv 5
rs121913243
MET
0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05 4
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 3