Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs11066132 1.000 0.040 12 112030402 intron variant C/T snv 5.8E-03 1
rs4767364 0.807 0.160 12 112083644 intron variant G/A snv 0.45 1