Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs157580 0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs10468017 0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs174570 0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9