Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs419137
CFH
1 196727745 intron variant G/T snv 0.92 1
rs10494745 1.000 0.040 1 196918327 missense variant G/A snv 8.0E-02 7.4E-02 1
rs10801582 1 196975227 upstream gene variant G/A snv 0.22 1
rs2786107 1 197341647 intron variant G/T snv 0.80 1
rs10754218 1 197195884 intron variant G/A snv 0.60 1