Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918005 0.925 0.080 1 21560662 missense variant C/G;T snv 4.0E-06; 1.2E-05 2
rs770093969 1.000 0.080 1 21560683 missense variant C/G;T snv 4.0E-06; 1.2E-05 1
rs1470389268 1.000 0.080 1 21560716 missense variant C/T snv 4.0E-06 7.0E-06 1
rs121918001 0.882 0.080 1 21561126 missense variant C/A;T snv 3
rs121918003 0.925 0.080 1 21561127 missense variant G/A;C snv 4.0E-06; 1.2E-05 2
rs1304394441 1.000 0.080 1 21561138 missense variant G/A snv 1
rs1057521085 1.000 0.080 1 21561142 missense variant A/G snv 7.0E-06 1
rs121918015 0.882 0.160 1 21563135 missense variant C/T snv 2
rs773257111 1.000 0.080 1 21563143 missense variant G/A snv 8.0E-06 7.0E-06 1
rs121918013 0.827 0.120 1 21563158 missense variant G/A snv 5
rs954135116 1.000 0.080 1 21563170 missense variant G/A snv 4.0E-06 1
rs1159854007 1.000 0.080 1 21563194 missense variant G/A snv 7.0E-06 1
rs786204530 0.851 0.160 1 21563212 missense variant AC/CA mnv 3
rs780583917 1.000 0.080 1 21563213 missense variant C/A snv 5.2E-05 6.3E-05 1
rs121918011 0.851 0.080 1 21563219 missense variant G/A;C snv 1.4E-04 4
rs1376937780 1.000 0.080 1 21563255 missense variant C/T snv 1
rs149344982 1.000 0.080 1 21563267 missense variant G/A snv 1.2E-02 8.6E-03 1
rs760029254 1.000 0.080 1 21564052 missense variant G/A snv 1.6E-05 1
rs121918012 1.000 0.080 1 21564053 missense variant G/T snv 1
rs778232217 1.000 0.080 1 21564080 missense variant A/G snv 8.0E-06 1
rs121918019 0.882 0.080 1 21564094 missense variant G/A;C snv 9.2E-05 3
rs199669988 0.882 0.080 1 21564097 missense variant G/A snv 1.3E-04 3.5E-05 3
rs121918000 0.925 0.080 1 21564103 missense variant G/A snv 1.2E-05 2
rs199590449 0.925 0.080 1 21564110 missense variant C/T snv 4.0E-05 7.0E-06 2
rs763159520 0.925 0.080 1 21564118 missense variant C/T snv 1.2E-05 7.0E-06 2