Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1059312 1.000 0.080 12 128794319 synonymous variant A/G snv 0.44 0.43 1
rs11059919 1.000 0.080 12 128804645 intron variant G/A snv 0.52 1
rs11059927 1.000 0.080 12 128809788 non coding transcript exon variant T/C snv 9.1E-02 1
rs1385374 1.000 0.080 12 128816149 intron variant C/T snv 9.1E-02 1