Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738491 0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs2143571 0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs74315468 0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs626283 0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs1420472625 0.925 0.040 19 54178800 missense variant G/C snv 2
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs56225452 0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs4240624 0.882 0.040 8 9326721 intron variant G/A snv 0.87 5