Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250259 1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs17517928
FN1
1.000 0.040 2 215426636 intron variant C/T snv 0.24 1