Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799977 0.662 0.440 3 37012077 missense variant A/C;G;T snv 0.23 28
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1800751 0.851 0.160 17 43047676 missense variant G/A;C snv 4.0E-06 5
rs1801200 0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs200928781 0.752 0.240 22 28695800 missense variant T/A;C;G snv 2.4E-05 11
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2066827 0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2228611 0.708 0.520 19 10156401 synonymous variant T/A;C snv 0.52 19
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs273900729 0.925 0.160 17 43082529 missense variant A/G snv 2
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 16
rs28897696 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 11
rs28997576 0.776 0.160 2 214752454 missense variant C/G;T snv 1.5E-02 11
rs3177427 0.827 0.160 14 77326864 stop gained G/A;C;T snv 5
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 14
rs41293459 0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 12
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55