Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs17366568
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs731839
PEPD
19 33408159 intron variant G/A snv 0.63 5
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs7193788 0.925 0.120 16 82622555 upstream gene variant A/G snv 0.16 4
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs6450176
ARL15
5 54002195 intron variant G/A snv 0.27 4
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs1656930 1.000 0.080 3 186835068 intergenic variant A/G snv 0.86 3
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 3
rs12051272
CDH13
0.925 0.120 16 82629683 intron variant G/C;T snv 3
rs4783244
CDH13
0.925 0.120 16 82628663 intron variant G/T snv 0.38 3
rs2590838
PBRM1
3 52588070 intron variant G/A snv 0.55 3
rs6773957
ADIPOQ ; ADIPOQ-AS1
1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55 2
rs4311394
ARL15
1.000 0.080 5 54004832 intron variant A/G snv 0.27 2
rs1108842
GNL3 ; PBRM1
3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 2
rs10447248 5 108580035 intergenic variant A/G snv 0.70 1
rs10794657 1 24299684 intergenic variant A/G snv 0.75 1
rs11005497 10 56750178 intergenic variant A/C snv 0.14 1