Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520012 1.000 0.040 4 65404419 missense variant C/T snv 1
rs199614818 1.000 0.040 4 65490529 missense variant C/A;T snv 4.0E-06; 2.4E-05 1