Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3817334 1.000 0.080 11 47629441 intron variant C/T snv 0.36 7
rs7531118 1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs3101336 1.000 0.080 1 72285502 intron variant T/C snv 0.62 6