Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9905742 1.000 0.080 17 4539780 missense variant T/A snv 3.0E-02 2.7E-02 1
rs9376268 0.925 0.080 6 137211614 intron variant G/A snv 0.20 2
rs9376267 0.925 0.080 6 137209894 5 prime UTR variant C/T snv 0.22 2
rs9272785 0.882 0.080 6 32642624 missense variant G/A snv 0.18 8.7E-02 3
rs9272461 1.000 0.080 6 32637832 intron variant G/A snv 0.13 1
rs9271300 1.000 0.080 6 32613805 intergenic variant C/G snv 0.54 1
rs9061 0.925 0.080 2 230212395 missense variant C/T snv 0.11 9.1E-02 2
rs897200 0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54 4
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs8177374 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs7958311 0.851 0.160 12 121167552 missense variant G/A;C snv 0.25; 4.0E-06 5
rs7873784 0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs779826162 0.925 0.080 4 38796574 missense variant C/T snv 2.0E-05 1.4E-05 2
rs7749390 0.882 0.120 6 137219233 5 prime UTR variant A/G;T snv 0.43; 4.4E-06 3
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs7518660 0.925 0.120 1 67219760 intron variant G/A snv 0.43 0.47 2
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs722555 1.000 0.080 2 230168800 non coding transcript exon variant C/T snv 0.57 1
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs7095891 0.882 0.120 10 52771701 upstream gene variant G/A snv 0.30 3