Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1150752 0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02 3
rs12566340 0.925 0.200 1 113877706 3 prime UTR variant C/A;T snv 3
rs147846074 0.925 0.200 21 44289743 missense variant C/G;T snv 1.2E-05; 3.2E-05; 4.0E-06 3
rs154981 0.925 0.200 6 32913216 regulatory region variant C/A;G;T snv 2
rs17879469 0.763 0.360 6 32584333 missense variant C/G snv 1.3E-05 9
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs185819 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs204990 0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs2071554 0.925 0.200 6 32816899 missense variant C/A;T snv 4.1E-06; 6.2E-02 2
rs2227956 0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 12
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2244839 0.882 0.200 6 31470591 non coding transcript exon variant G/A;T snv 3
rs2256965 0.925 0.200 6 31587353 non coding transcript exon variant A/G;T snv 0.60 2
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2488457 0.763 0.480 1 113872746 intron variant G/A;C snv 11
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3129941 0.882 0.240 6 32369909 missense variant A/G;T snv 0.81 3