Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5
rs6450176
ARL15
5 54002195 intron variant G/A snv 0.27 3
rs2590838
PBRM1
3 52588070 intron variant G/A snv 0.55 3
rs731839
PEPD
19 33408159 intron variant G/A snv 0.63 3
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 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
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 1
rs11168618 12 48539450 intergenic variant C/T snv 0.33 1
rs1515110 2 226257500 intergenic variant G/A;C;T snv 1
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 1
rs2468677 8 139507274 downstream gene variant G/T snv 0.54 1
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 1
rs62309628 4 73014333 intergenic variant G/C snv 0.10 1
rs6810075 3 186830776 downstream gene variant T/C snv 0.37 1
rs7955516 12 20345102 intergenic variant A/C;G;T snv 1
rs822354 3 186762417 intron variant A/G snv 0.72 1
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 1
rs925735 2 226314914 intergenic variant C/G snv 0.66 1
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs17366568
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 1