Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs117026326 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10