Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1554888939 0.683 0.640 9 137798823 missense variant G/T snv 58
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs267606959 0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 19
rs1014959895 0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1251713297 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs1553403917 0.807 0.320 2 73451171 frameshift variant -/A delins 7
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs779021719 0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 5
rs12784396 0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 4