Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs174541 1.000 0.080 11 61798436 intron variant T/C snv 0.29 8