Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11229 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs3115663 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 6
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs9268832 0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 4
rs204994 0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 3
rs7192 0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 3