Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 3
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 6
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs3865014 0.851 0.080 15 69269179 missense variant G/A snv 0.75 0.69 1
rs5743810 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 1
rs9306160 0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 2
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs2290854 0.925 0.080 1 204546897 intron variant A/G snv 0.65 0.57 1
rs592373 0.925 0.080 11 1869760 intron variant G/A;T snv 0.63; 6.8E-06 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 1
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 1
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs2227928
ATR
0.851 0.200 3 142562770 missense variant A/G snv 0.55 0.63 1
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 4
rs2073618 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 1
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 8
rs280519 0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 1
rs2363956 0.776 0.160 19 17283315 missense variant T/G snv 0.48 0.50 4
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 8
rs8100241 0.827 0.120 19 17282085 missense variant G/A snv 0.47 0.47 2