Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53