Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs11571818 0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92