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: rs28940284
rs28940284
1 1.000 0.040 1 20644526 missense variant C/A;T snv 4.0E-06 0.800 1.000 21 2004 2014
dbSNP: rs28940285
rs28940285
1 1.000 0.040 1 20645640 missense variant T/C snv 1.6E-05 3.5E-05 0.800 1.000 21 2004 2014
dbSNP: rs74315355
rs74315355
1 0.790 0.080 1 20644639 missense variant G/A snv 0.800 1.000 21 2004 2014
dbSNP: rs74315358
rs74315358
1 1.000 0.040 1 20644549 missense variant G/A snv 4.4E-05 7.7E-05 0.800 1.000 21 2004 2014
dbSNP: rs74315359
rs74315359
1 0.882 0.040 1 20644651 missense variant C/T snv 2.0E-05 1.4E-05 0.800 1.000 21 2004 2014
dbSNP: rs74315360
rs74315360
1 0.925 0.040 1 20638104 missense variant C/A snv 0.800 1.000 21 2004 2014
dbSNP: rs573931674
rs573931674
1 1.000 0.040 1 20639934 missense variant G/A snv 4.0E-06 0.710 0.952 20 2004 2014
dbSNP: rs372280083
rs372280083
1 1.000 0.040 1 20644515 missense variant C/G snv 9.5E-05 5.6E-05 0.700 1.000 20 2004 2014
dbSNP: rs556540177
rs556540177
1 1.000 0.040 1 20648601 missense variant G/A;C;T snv 1.0E-04; 4.0E-06; 1.6E-05 0.700 1.000 20 2004 2014
dbSNP: rs764328076
rs764328076
1 1.000 0.040 1 20649134 missense variant G/A snv 2.4E-05 7.0E-06 0.700 1.000 20 2004 2014
dbSNP: rs768091663
rs768091663
1 1.000 0.040 1 20637956 missense variant G/C snv 2.0E-05 0.700 1.000 20 2004 2014
dbSNP: rs772510148
rs772510148
1 1.000 0.040 1 20644551 missense variant G/A snv 4.4E-05 2.1E-05 0.700 1.000 20 2004 2014
dbSNP: rs775809722
rs775809722
1 1.000 0.040 1 20633925 missense variant A/C;G snv 5.3E-06; 3.7E-05 0.700 1.000 20 2004 2014
dbSNP: rs138302371
rs138302371
1 1.000 0.040 1 20638041 missense variant C/T snv 1.9E-04 1.7E-04 0.700 1.000 1 2013 2013
dbSNP: rs1195888869
rs1195888869
1 1.000 0.040 1 20645706 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs138050841
rs138050841
1 0.925 0.040 1 20637894 missense variant G/A snv 2.0E-05 3.5E-05 0.700 0