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: rs63750231
rs63750231
23 0.689 0.160 14 73198100 missense variant A/C;G snv 0.030 1.000 3 2000 2016
dbSNP: rs17125721
rs17125721
14 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 0.020 1.000 2 2005 2019
dbSNP: rs63749824
rs63749824
8 0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.020 1.000 2 2007 2016
dbSNP: rs765670175
rs765670175
7 0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 0.020 1.000 2 2006 2008
dbSNP: rs112451138
rs112451138
2 0.925 0.080 14 73192667 missense variant T/C snv 7.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs63749835
rs63749835
5 0.851 0.080 14 73192799 missense variant T/C snv 0.010 1.000 1 2017 2017
dbSNP: rs63750004
rs63750004
4 0.851 0.080 14 73173655 missense variant T/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs63750082
rs63750082
13 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs63750083
rs63750083
13 0.732 0.160 14 73219177 missense variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs63750324
rs63750324
2 0.925 0.080 14 73198111 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs63750444
rs63750444
4 0.882 0.080 14 73192745 missense variant G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs63750687
rs63750687
33 0.752 0.200 14 73217137 missense variant C/A;G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs63750802
rs63750802
7 0.851 0.080 14 73219144 missense variant T/G snv 0.010 1.000 1 2013 2013
dbSNP: rs63750900
rs63750900
9 0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 1997 1997
dbSNP: rs63750907
rs63750907
6 0.807 0.120 14 73173667 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs63751032
rs63751032
7 0.851 0.080 14 73219156 missense variant T/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs63751037
rs63751037
7 0.790 0.080 14 73173642 missense variant A/G snv 0.010 1.000 1 1998 1998
dbSNP: rs63751068
rs63751068
6 0.827 0.120 14 73186920 missense variant G/C;T snv 0.010 1.000 1 2004 2004
dbSNP: rs63751399
rs63751399
3 0.882 0.120 14 73171047 missense variant T/A;C snv 0.010 1.000 1 2000 2000