Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 12
rs2067087 1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs4823006 22 29055683 3 prime UTR variant A/G snv 0.41 5
rs34322 12 12726636 intron variant T/C snv 0.50 2