Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 138
rs1801282 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 77
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 74
rs662 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 71
rs1260326 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 63
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
rs738409 0.590 0.536 22 43928847 missense variant C/G snp 0.28 0.22 55
rs4994 0.605 0.536 8 37966280 missense variant A/G snp 0.11 9.0E-02 44
rs56149945 0.626 0.643 5 143399752 missense variant T/A,C snp 2.0E-02 2.2E-02 35
rs3856806 0.715 0.357 3 12434058 synonymous variant C/T snp 0.13 0.13 18
rs1800797 0.692 0.464 7 22726602 non coding transcript exon variant A/G snp 0.69 16
rs80356624 0.734 0.250 11 17387490 missense variant C/A,T snp 15
rs4402960 0.756 0.286 3 185793899 intron variant G/T snp 0.38 12
rs1387153 0.769 0.250 11 92940662 intergenic variant C/G,T snp 0.33 10
rs137853240 0.801 0.071 12 120994405 missense variant G/A snp 7
rs121909244 0.821 0.107 3 12434111 missense variant C/A,T snp 4.0E-06 7
rs10010131 0.821 0.107 4 6291188 intron variant A/G snp 0.66 0.63 6
rs7608798 0.878 0.107 2 162033707 intron variant G/A snp 0.34 5
rs193922289
GCK
0.821 0.214 7 44152420 missense variant C/T snp 4.0E-06 5
rs193929375
GCK
0.821 0.214 7 44145560 missense variant C/A snp 5
rs11554159 0.846 0.179 19 18175134 missense variant G/A snp 0.23 0.24 5
rs561017686 0.878 0.107 2 181678138 missense variant G/A,C snp 8.0E-06; 8.4E-04 3.2E-05; 3.2E-05 4
rs1055419 0.878 0.071 3 125594988 5 prime UTR variant G/A snp 7.0E-02 4
rs587777042 0.878 0.036 8 144096615 missense variant C/T snp 4.0E-06 3