Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555743003 0.701 0.520 18 33740444 splice donor variant G/A snv 58
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs866294686 0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 39
rs1178187217 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 38
rs201943194 0.683 0.480 7 21710596 stop gained C/T snv 8.5E-05 8.4E-05 38
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 36
rs1034395178 0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 28
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs137854539 0.716 0.520 20 58903703 missense variant C/T snv 27
rs1294950721 0.807 0.360 20 10645355 splice donor variant C/A;T snv 7.0E-06 27
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs559979281 0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04 23
rs863225422 0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs1557055405 0.807 0.400 X 153743532 missense variant T/A snv 21
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 19
rs1441937959 0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 19
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 18
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 17
rs74597325 0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 16
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 14