Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 2
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 1
rs4754373 11 109022119 intron variant C/T snv 0.21 1
rs534870 1.000 0.080 13 80385072 intergenic variant G/A snv 0.71 1
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48 1
rs2605100
LOC107985272 ; LYPLAL1-AS1
1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 1
rs2245667
PDGFRL
8 17603819 intron variant C/G snv 0.64 1
rs6429082
TBCE
1.000 0.080 1 235436814 intron variant T/C snv 0.55 1