Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs171748 1.000 0.040 5 61203304 intron variant A/G snv 0.60 2
rs256377 5 61210447 intron variant A/G snv 0.59 1
rs62366190 5 61188108 intron variant C/G snv 0.25 1
rs159544 5 61193420 intron variant A/C;G snv 1
rs194369 5 61203358 intron variant A/G snv 0.47 1