Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs528557 0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29 6
rs3918396 0.851 0.120 20 3671118 missense variant C/T snv 5.1E-05; 7.6E-02 6.7E-02 5
rs2280090 0.882 0.120 20 3669558 missense variant G/A snv 0.13 0.14 4