Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17367504 1.000 0.040 1 11802721 intron variant A/G snv 0.14 3
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs4846049 0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 1
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1