Disease: Obesity
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs4783819
FTO
0.925 0.120 16 53782735 intron variant G/C snv 0.68 3
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
rs12152703
KLB
0.925 0.120 4 39420199 intron variant G/T snv 0.28 2
rs7674434
KLB
0.925 0.120 4 39417789 intron variant T/G snv 0.32 2
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39