Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs4612666 0.763 0.440 1 247435768 intron variant T/C snv 0.65 10
rs2234671 0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs747753882 0.925 0.120 4 38797482 synonymous variant A/G snv 4.0E-06 2.1E-05 3