Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80358306 1.000 0.080 11 68357679 missense variant C/T snv 3.9E-04 5.0E-04 1
rs80358317 1.000 0.080 11 68425226 missense variant A/G snv 6.4E-04 2.4E-04 1
rs369471051 1.000 11 68413958 missense variant C/T snv 5.7E-05 7.0E-05 1
rs377258285 1.000 0.120 11 68425202 missense variant C/T snv 5.6E-05 6.3E-05 1
rs201030241 1.000 0.080 11 68446497 missense variant A/G snv 3.7E-04 5.6E-05 1
rs80358320 1.000 0.080 11 68436969 missense variant T/G snv 2.0E-05 3.5E-05 1
rs1273567061 1.000 0.120 11 68386525 missense variant A/G snv 4.0E-06 2.1E-05 1
rs80358316 1.000 0.080 11 68411509 missense variant A/G snv 8.0E-06 2.1E-05 1
rs757888034 1.000 0.120 11 68386600 missense variant G/A;T snv 1.2E-05; 4.0E-06 1.4E-05 1
rs765952535 1.000 0.080 11 68411530 missense variant C/T snv 1.6E-05 1.4E-05 1
rs1339222045 1.000 11 68406773 missense variant T/C snv 1.2E-05 1.4E-05 1
rs373910016 0.882 0.120 11 68386660 missense variant G/A snv 4.0E-06 1.4E-05 1
rs1219101402 1.000 0.120 11 68365607 missense variant C/T snv 7.0E-06 1
rs376152274 1.000 0.080 11 68386621 missense variant G/A snv 4.0E-06 7.0E-06 1
rs1320065036 0.925 0.160 11 68386342 missense variant C/T snv 4.0E-06 7.0E-06 2
rs80358308 0.925 0.080 11 68386630 missense variant C/T snv 2.0E-05 7.0E-06 1
rs1398692057 1.000 0.080 11 68413740 missense variant C/T snv 7.0E-06 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
rs80358311 1.000 0.080 11 68403546 missense variant G/A snv 4.0E-06 7.0E-06 1
rs80358312 0.925 0.080 11 68403607 missense variant G/A snv 7.0E-06 1
rs866606166 1.000 0.120 11 68386678 missense variant G/A snv 7.0E-06 1
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
rs201320326 1.000 0.120 11 68386499 missense variant C/A;T snv 2.2E-04 1