Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs3782886 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs3782889 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 2
rs4766566 0.851 0.200 12 111269073 intron variant C/T snv 0.42 2