Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174570 0.882 0.200 11 61829740 intron variant C/T snv 0.15 10
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs9261290 0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs2068834 0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 9
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 9
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9