Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6235 0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs6234 0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs6232 0.925 0.080 5 96416081 missense variant T/C snv 3.9E-02 3.2E-02 2
rs750845408 0.925 0.080 5 96423317 missense variant T/C snv 4.5E-05 7.0E-05 2
rs155971 1.000 0.080 5 96414692 intron variant T/C snv 0.57 1
rs765019354 1.000 0.080 5 96429260 stop gained G/A;C snv 4.0E-06; 1.6E-05 1