Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78490412 1.000 0.040 2 143405256 intron variant C/T snv 0.22 1
rs13010737 1.000 0.040 2 143442474 intron variant G/A snv 0.36 1
rs6734367 2 143556678 intron variant T/A;G snv 1
rs74847330 2 143074030 intergenic variant A/G snv 8.8E-02 4
rs73962318 2 143097365 non coding transcript exon variant T/C snv 4.2E-02 2