Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs4648318 1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs1075650 9 129176634 3 prime UTR variant T/C snv 0.25 1
rs1875999 5 76969157 3 prime UTR variant T/C snv 0.38 1
rs702764 0.925 0.120 8 53229597 synonymous variant T/C;G snv 0.17; 8.0E-06 4