Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057519942
rs1057519942
15 0.724 0.320 3 179203760 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs121913281
rs121913281
37 0.623 0.520 3 179234296 missense variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs121913283
rs121913283
14 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs121913285
rs121913285
1 3 179218286 missense variant C/G snv 0.700 1.000 1 2014 2014
dbSNP: rs121913288
rs121913288
1 1.000 0.200 3 179234219 missense variant A/G snv 0.700 1.000 1 2014 2014
dbSNP: rs587777790
rs587777790
12 0.732 0.280 3 179199690 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs867262025
rs867262025
9 0.790 0.360 3 179221146 missense variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs104886003
rs104886003
34 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.710 1.000 12 2004 2016
dbSNP: rs121913279
rs121913279
45 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.740 1.000 10 2004 2016