Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs180177135 0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 27
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 21
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 19
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19