Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23