Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4594881 1.000 0.080 5 35846713 intergenic variant G/T snv 0.28 2
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3
rs61894547 0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs7918084 1.000 0.080 10 92669710 non coding transcript exon variant C/T snv 0.60 3
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs8005161 0.882 0.120 14 88006251 intron variant C/T snv 0.18 5
rs9807989 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2