Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10754218 1 197195884 intron variant G/A snv 0.60 1
rs10429910 1 197172123 intron variant A/C snv 0.28 0.21 1
rs7410943 1 197185891 intron variant A/G snv 0.44 1
rs1415212 1 197188764 intron variant T/A snv 0.26 1