Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs993226 0.851 0.160 12 84492794 intergenic variant T/G snv 6.3E-02 4
rs941934 0.851 0.200 1 152417976 intron variant T/A;C snv 5
rs9357733 0.851 0.160 6 52427338 intron variant A/G snv 0.19 4
rs7936562 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 4
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs7534334 0.882 0.160 1 153205376 downstream gene variant C/T snv 0.25 3
rs7518129 0.882 0.120 1 173194429 intron variant A/G snv 0.47 3
rs73196739
LPP
0.925 0.120 3 188684683 intron variant C/T snv 0.13 2
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs7124842 0.882 0.160 11 76600576 intergenic variant G/A;C;T snv 3
rs712484 0.882 0.160 14 48081576 intergenic variant C/A snv 0.14 3
rs6894249 0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45 9
rs6693927 0.925 0.120 1 153071533 upstream gene variant G/A snv 0.35 2
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs62623446 0.882 0.120 12 54974507 missense variant C/T snv 4.5E-02 4.4E-02 3
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs574456 0.882 0.160 2 140644133 intron variant A/T snv 8.1E-02 3
rs5744292 0.851 0.200 11 112143413 3 prime UTR variant T/C snv 0.16 4