Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1057520001 0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs5030824
VHL
0.776 0.320 3 10149885 missense variant C/G snv 2.0E-05 4.2E-05 9
rs587777894 0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs121913243
MET
0.827 0.160 7 116777410 missense variant A/C;G snv 1.2E-05 7
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 7
rs1049380 0.827 0.120 12 26336611 3 prime UTR variant G/T snv 0.69 5
rs7105934 0.827 0.120 11 69424973 upstream gene variant G/A;C snv 5