Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs205764 1.000 0.080 7 130913477 intron variant G/T snv 0.65 1
rs157928 1.000 0.040 7 130896599 intron variant T/C snv 0.29 1
rs547311 1.000 0.080 7 130913695 intron variant G/A snv 0.31 1