Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs1108842
GNL3 ; PBRM1
3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 2
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 2
rs11924390
LOC105374258
3 186715310 intron variant T/A;C snv 1
rs12051272
CDH13
0.925 0.120 16 82629683 intron variant G/C;T snv 1
rs1515110 2 226257500 intergenic variant G/A;C;T snv 1
rs7955516 12 20345102 intergenic variant A/C;G;T snv 1
rs889140
PEPD
19 33398094 intron variant G/A;C snv 1
rs17366568
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 1
rs62309628 4 73014333 intergenic variant G/C snv 0.10 1
rs4301033
LINC01214 ; LOC107986141
3 150324831 regulatory region variant G/A snv 0.12 1
rs4311394
ARL15
1.000 0.080 5 54004832 intron variant A/G snv 0.27 1
rs6450176
ARL15
5 54002195 intron variant G/A snv 0.27 3
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
rs3001032
LYPLAL1-AS1
1 219554437 upstream gene variant T/C snv 0.35 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 5
rs6810075 3 186830776 downstream gene variant T/C snv 0.37 1
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs4783244
CDH13
0.925 0.120 16 82628663 intron variant G/T snv 0.38 1
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 1
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs2468677 8 139507274 downstream gene variant G/T snv 0.54 1
rs2590838
PBRM1
3 52588070 intron variant G/A snv 0.55 3