Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs5744168 0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs4958881 0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs10127939 0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5