Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1570204 9 4216751 intron variant T/C snv 0.25 1
rs2224492 9 4237546 intron variant A/G snv 0.25 1
rs6476827 9 4220832 intron variant C/G snv 0.24 1
rs7047871 9 4050113 intron variant T/A snv 0.30 1