Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918013 0.827 0.120 1 21563158 missense variant G/A snv 5
rs121918002 0.851 0.080 1 21573683 missense variant A/C snv 3.6E-05 7.0E-05 4
rs121918007 0.851 0.080 1 21564139 missense variant G/A;C snv 2.4E-03; 4.0E-06 4
rs121918008 0.851 0.080 1 21575868 missense variant A/T snv 4.0E-06 7.0E-06 4
rs121918009 0.851 0.080 1 21575736 missense variant G/A snv 4
rs121918011 0.851 0.080 1 21563219 missense variant G/A;C snv 1.4E-04 4
rs121918001 0.882 0.080 1 21561126 missense variant C/A;T snv 3
rs121918010 0.827 0.200 1 21573781 missense variant T/C snv 7.2E-05 4.2E-05 3
rs121918014 0.827 0.120 1 21576582 missense variant A/G snv 2.0E-05 5.6E-05 3
rs121918018 0.882 0.120 1 21568201 missense variant G/C;T snv 1.6E-05; 4.0E-06 3
rs121918019 0.882 0.080 1 21564094 missense variant G/A;C snv 9.2E-05 3
rs1413274209 0.882 0.080 1 21577544 missense variant G/A snv 8.3E-06 2.1E-05 3
rs199669988 0.882 0.080 1 21564097 missense variant G/A snv 1.3E-04 3.5E-05 3
rs371243939 0.882 0.080 1 21575906 missense variant C/T snv 1.2E-05 1.4E-05 3
rs766076920 0.882 0.080 1 21568122 missense variant C/T snv 8.0E-06 2.1E-05 3
rs781272386 0.882 0.080 1 21570327 missense variant G/A;C;T snv 8.0E-06; 4.0E-06; 8.0E-06 3
rs786204530 0.851 0.160 1 21563212 missense variant AC/CA mnv 3
rs121918000 0.925 0.080 1 21564103 missense variant G/A snv 1.2E-05 2
rs121918003 0.925 0.080 1 21561127 missense variant G/A;C snv 4.0E-06; 1.2E-05 2
rs121918004 0.925 0.080 1 21564188 missense variant A/C snv 2
rs121918005 0.925 0.080 1 21560662 missense variant C/G;T snv 4.0E-06; 1.2E-05 2
rs121918006 0.925 0.080 1 21576638 missense variant T/C snv 2
rs121918015 0.882 0.160 1 21563135 missense variant C/T snv 2
rs1442918125 0.925 0.080 1 21575907 missense variant G/A snv 8.0E-06 7.0E-06 2
rs199590449 0.925 0.080 1 21564110 missense variant C/T snv 4.0E-05 7.0E-06 2