Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10207628 0.925 0.120 2 127094445 intron variant G/A;C snv 2
rs10194375 1.000 0.080 2 127082205 intron variant C/A;T snv 1
rs1060743 0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 1
rs17014873 1.000 0.080 2 127072643 intron variant A/C snv 0.11 1
rs6431219 1.000 0.080 2 127104557 intron variant C/T snv 0.41 1
rs72838215 1.000 0.080 2 127104478 intron variant G/A snv 0.13 1