Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908670 0.882 0.080 11 68363784 missense variant G/A snv 3
rs80358313 0.882 0.160 11 68406550 missense variant G/A;C;T snv 1.2E-05; 1.2E-05; 3.2E-05 2
rs1320065036 0.925 0.160 11 68386342 missense variant C/T snv 4.0E-06 7.0E-06 2
rs866606166 1.000 0.120 11 68386678 missense variant G/A snv 7.0E-06 1
rs201320326 1.000 0.120 11 68386499 missense variant C/A;T snv 2.2E-04 1
rs121908665 1.000 0.120 11 68403606 missense variant C/T snv 1
rs121908664 1.000 0.120 11 68389949 missense variant G/A snv 1
rs1318906451 1.000 0.120 11 68389900 missense variant T/A snv 4.0E-06 1
rs397514665 1.000 0.120 11 68363791 missense variant C/T snv 1.2E-05 1
rs377258285 1.000 0.120 11 68425202 missense variant C/T snv 5.6E-05 6.3E-05 1
rs746701187 1.000 0.120 11 68410019 missense variant T/C snv 4.0E-06 1
rs545508982 1.000 0.120 11 68389980 stop gained G/A;T snv 4.0E-06; 8.0E-06 1
rs757888034 1.000 0.120 11 68386600 missense variant G/A;T snv 1.2E-05; 4.0E-06 1.4E-05 1
rs750791263 1.000 0.120 11 68386510 missense variant G/A snv 1.2E-05 7.0E-06 1
rs760548029 1.000 0.120 11 68357768 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1273567061 1.000 0.120 11 68386525 missense variant A/G snv 4.0E-06 2.1E-05 1
rs1470530779 1.000 0.120 11 68406769 missense variant G/A snv 4.0E-06 1
rs1219101402 1.000 0.120 11 68365607 missense variant C/T snv 7.0E-06 1
rs1158745675 1.000 0.120 11 68386367 stop gained C/A;T snv 4.0E-06; 4.0E-06 1
rs121908671 0.851 0.120 11 68357801 missense variant G/A snv 1
rs121908672 0.925 0.080 11 68357802 missense variant C/T snv 1
rs121908669 1.000 0.040 11 68357672 missense variant G/C snv 1
rs121908673 0.925 0.160 11 68363818 missense variant C/T snv 1
rs201030241 1.000 0.080 11 68446497 missense variant A/G snv 3.7E-04 5.6E-05 1
rs1332274863 1.000 0.080 11 68386441 missense variant G/A snv 4.0E-06 1