Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs549858786 0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs562962093 0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs563558831 0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs5743293 0.807 0.200 16 50729868 frameshift variant C/-;CC delins 7
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs628977 0.851 0.160 20 3669074 intron variant T/C snv 0.65 4
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs72661131 0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs848 0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs528557 0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29 6
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs11465553 0.925 0.120 6 52236960 missense variant C/T snv 3.0E-02 3.0E-02 2
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs5063 0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16