Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 1
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 1
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 1
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 1
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 2
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 5
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4