Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83