Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
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
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
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs1805015 0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs5743810 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs11558538 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs4696480 0.716 0.400 4 153685974 intron variant T/A snv 0.45 19