Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs3825172 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs74421874 0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14