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: rs36053993
rs36053993
31 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 0.800 1.000 43 2002 2016
dbSNP: rs140342925
rs140342925
5 0.882 0.120 1 45332445 missense variant C/T snv 8.4E-05 8.4E-05 0.800 1.000 30 2002 2017
dbSNP: rs529008617
rs529008617
7 0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05 0.800 1.000 30 2002 2017
dbSNP: rs587782228
rs587782228
4 0.882 0.120 1 45330557 missense variant C/A;T snv 4.2E-06; 4.2E-06 0.800 1.000 29 2002 2017
dbSNP: rs34612342
rs34612342
32 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 0.800 1.000 23 2002 2017
dbSNP: rs374950566
rs374950566
2 1.000 0.120 1 45332215 missense variant G/A snv 1.2E-05 1.4E-05 0.800 1.000 23 2002 2016
dbSNP: rs34126013
rs34126013
3 0.925 0.160 1 45332458 missense variant G/A snv 6.8E-05 2.1E-05 0.800 1.000 22 2002 2016
dbSNP: rs769237459
rs769237459
2 1.000 0.120 1 45332279 missense variant G/A snv 8.0E-06 0.800 1.000 20 2002 2017
dbSNP: rs876659676
rs876659676
2 1.000 0.120 1 45332252 missense variant T/C snv 4.0E-06 1.4E-05 0.800 1.000 17 2002 2016
dbSNP: rs747993448
rs747993448
2 1.000 0.120 1 45332795 missense variant G/A snv 4.0E-06 2.8E-05 0.800 1.000 16 2004 2017
dbSNP: rs143353451
rs143353451
5 0.851 0.120 1 45332794 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 1.2E-05 0.800 1.000 14 2004 2017
dbSNP: rs730881833
rs730881833
6 0.827 0.160 1 45332242 missense variant C/A;T snv 4.0E-06; 2.8E-05 0.800 1.000 4 2007 2015
dbSNP: rs1057517765
rs1057517765
1 1.000 0.120 1 45332466 missense variant T/C;G snv 0.800 1.000 3 2008 2009
dbSNP: rs1060501335
rs1060501335
2 0.925 0.120 1 45331684 missense variant A/G snv 0.800 0
dbSNP: rs150792276
rs150792276
1 1.000 0.120 1 45331467 missense variant G/A snv 8.2E-04 8.0E-04 0.700 1.000 22 2002 2017
dbSNP: rs200844166
rs200844166
3 0.882 0.160 1 45331240 missense variant G/T snv 2.4E-05 5.6E-05 0.700 1.000 22 2002 2017
dbSNP: rs200872702
rs200872702
1 1.000 0.120 1 45332597 missense variant T/C snv 2.2E-04 8.4E-05 0.700 1.000 22 2002 2017
dbSNP: rs533899702
rs533899702
1 1.000 0.120 1 45332785 missense variant C/T snv 8.0E-06 7.0E-06 0.700 1.000 22 2002 2017
dbSNP: rs587782263
rs587782263
1 1.000 0.120 1 45331193 missense variant C/A;T snv 3.6E-05 6.3E-05 0.700 1.000 22 2002 2017
dbSNP: rs768553551
rs768553551
1 1.000 0.120 1 45332617 missense variant C/T snv 8.0E-06 0.700 1.000 22 2002 2017
dbSNP: rs777184451
rs777184451
1 1.000 0.120 1 45332952 missense variant G/A snv 4.0E-06 7.0E-06 0.700 1.000 22 2002 2017
dbSNP: rs587778541
rs587778541
3 0.925 0.120 1 45331219 inframe deletion CCT/- delins 9.5E-05 2.8E-05 0.700 1.000 20 2003 2015
dbSNP: rs754155145
rs754155145
4 0.925 0.120 1 45332773 missense variant C/A;T snv 4.0E-06 0.700 1.000 15 2002 2016
dbSNP: rs79777494
rs79777494
3 0.882 0.120 1 45334495 missense variant G/A snv 1.1E-03 4.9E-04 0.700 1.000 15 2002 2016
dbSNP: rs121908381
rs121908381
3 0.925 0.120 1 45331220 stop gained C/A snv 5.2E-05 7.0E-06 0.700 1.000 13 2002 2017