Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs797044485 0.851 0.160 1 156134832 missense variant G/A snv 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3829251 0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140