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: rs58982919
rs58982919
10 0.790 0.080 8 24956223 missense variant T/C snv 0.050 1.000 5 2002 2018
dbSNP: rs281865140
rs281865140
2 0.925 0.080 8 24955515 missense variant T/C;G snv 0.020 1.000 2 2006 2012
dbSNP: rs57105105
rs57105105
4 0.925 0.080 8 24953776 missense variant C/T snv 0.020 1.000 2 2004 2015
dbSNP: rs59443585
rs59443585
2 0.925 0.080 8 24955521 missense variant T/G snv 0.020 1.000 2 2006 2012
dbSNP: rs62636503
rs62636503
3 0.882 0.080 8 24953779 missense variant C/T snv 0.020 1.000 2 2015 2017
dbSNP: rs58332872
rs58332872
5 0.882 0.080 8 24956248 missense variant C/T snv 0.010 1.000 1 2019 2019
dbSNP: rs59101996
rs59101996
2 0.925 0.080 8 24956070 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs62636505
rs62636505
2 0.925 0.080 8 24956235 missense variant A/G snv 0.010 1.000 1 2007 2007
dbSNP: rs62636522
rs62636522
1 1.000 0.080 8 24955877 missense variant G/A;C snv 4.1E-06; 7.2E-04 0.010 1.000 1 2006 2006