Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057521085 1.000 0.080 1 21561142 missense variant A/G snv 7.0E-06 1
rs1159854007 1.000 0.080 1 21563194 missense variant G/A snv 7.0E-06 1
rs1196976671 1.000 0.080 1 21577475 missense variant G/A snv 7.0E-06 1
rs121918000 0.925 0.080 1 21564103 missense variant G/A snv 1.2E-05 2
rs121918001 0.882 0.080 1 21561126 missense variant C/A;T snv 3
rs121918002 0.851 0.080 1 21573683 missense variant A/C snv 3.6E-05 7.0E-05 4
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
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
rs121918010 0.827 0.200 1 21573781 missense variant T/C snv 7.2E-05 4.2E-05 3
rs121918011 0.851 0.080 1 21563219 missense variant G/A;C snv 1.4E-04 4
rs121918012 1.000 0.080 1 21564053 missense variant G/T snv 1
rs121918013 0.827 0.120 1 21563158 missense variant G/A snv 5
rs121918014 0.827 0.120 1 21576582 missense variant A/G snv 2.0E-05 5.6E-05 3
rs121918015 0.882 0.160 1 21563135 missense variant C/T snv 2
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
rs1220125702 1.000 0.080 1 21573686 missense variant T/C snv 8.0E-06 7.0E-06 1
rs1223142821 1.000 0.080 1 21568193 missense variant G/T snv 4.0E-06 1
rs1304394441 1.000 0.080 1 21561138 missense variant G/A snv 1
rs1376937780 1.000 0.080 1 21563255 missense variant C/T snv 1