Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs1041740 0.807 0.320 21 31667849 intron variant C/T snv 0.24 8