Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14