Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11575886 1.000 0.080 20 56248494 upstream gene variant A/G snv 8.0E-02 1
rs17009726 1.000 0.080 2 118967884 intron variant A/G snv 1.0E-02 1
rs370738284 1.000 0.080 4 38797857 synonymous variant A/G snv 1.4E-05 1
rs3774275 1.000 0.080 3 187247480 intron variant A/G snv 0.22 1
rs3819545
VDR
1.000 0.080 12 47871223 intron variant A/G snv 0.36 1
rs6507226 1.000 0.080 18 22611328 intergenic variant A/G snv 0.45 1
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2069718 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs414171 0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs1554286 0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs7749390 0.882 0.120 6 137219233 5 prime UTR variant A/G;T snv 0.43; 4.4E-06 3
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs11568350 0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs656612 1.000 0.080 12 121138849 intron variant C/A snv 0.60 1
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs1136452 0.925 0.120 10 79612410 missense variant C/A;G;T snv 4.0E-06; 7.0E-03; 4.0E-06 2
rs4988453 0.851 0.200 3 38137763 upstream gene variant C/A;T snv 4
rs2393799 0.882 0.200 12 121132209 upstream gene variant C/A;T snv 3
rs12596308 0.925 0.120 16 29679875 intron variant C/A;T snv 2
rs2011839 1.000 0.080 2 118985008 intron variant C/A;T snv 1
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193