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: rs121917808
rs121917808
3 0.882 0.080 14 73219192 missense variant C/A snv 0.010 1.000 1 1998 1998
dbSNP: rs63749925
rs63749925
3 0.882 0.080 14 73219191 missense variant C/T snv 0.010 1.000 1 1999 1999
dbSNP: rs63750083
rs63750083
13 0.732 0.160 14 73219177 missense variant C/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs63751032
rs63751032
7 0.851 0.080 14 73219156 missense variant T/A;G snv 0.010 1.000 1 2007 2007
dbSNP: rs63750802
rs63750802
7 0.851 0.080 14 73219144 missense variant T/G snv 0.010 1.000 1 2007 2007
dbSNP: rs63751254
rs63751254
4 0.851 0.160 14 73217210 missense variant A/G snv 0.010 1.000 1 2000 2000
dbSNP: rs63750929
rs63750929
4 0.882 0.080 14 73217177 missense variant G/T snv 0.030 1.000 3 2008 2020
dbSNP: rs63751416
rs63751416
2 0.925 0.080 14 73217170 missense variant C/G snv 0.010 1.000 1 1999 1999
dbSNP: rs63750646
rs63750646
6 0.807 0.120 14 73217147 missense variant G/C snv 0.010 1.000 1 1999 1999
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: rs17125721
rs17125721
14 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 0.040 0.500 4 2000 2013
dbSNP: rs63751235
rs63751235
6 0.807 0.120 14 73198117 missense variant C/G snv 0.010 1.000 1 2001 2001
dbSNP: rs63749937
rs63749937
2 0.925 0.080 14 73198105 missense variant C/G;T snv 0.010 1.000 1 2001 2001
dbSNP: rs63750231
rs63750231
23 0.689 0.160 14 73198100 missense variant A/C;G snv 0.050 1.000 5 1997 2016
dbSNP: rs63750524
rs63750524
2 1.000 0.080 14 73198095 missense variant A/C snv 0.010 1.000 1 2007 2007
dbSNP: rs63749891
rs63749891
5 0.851 0.080 14 73198094 missense variant G/C;T snv 0.010 1.000 1 1997 1997
dbSNP: rs63751019
rs63751019
3 0.925 0.080 14 73198066 missense variant C/G snv 0.020 1.000 2 1996 2004
dbSNP: rs1179768627
rs1179768627
2 0.925 0.080 14 73198064 missense variant T/G snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs63750248
rs63750248
2 0.925 0.080 14 73198047 missense variant G/A;C;T snv 4.0E-06; 2.4E-05 0.010 1.000 1 1997 1997
dbSNP: rs63751320
rs63751320
1 1.000 0.080 14 73192862 missense variant A/C snv 0.010 1.000 1 2003 2003
dbSNP: rs63750888
rs63750888
2 0.925 0.080 14 73192828 missense variant A/C snv 0.010 1.000 1 2006 2006
dbSNP: rs63749835
rs63749835
5 0.851 0.080 14 73192799 missense variant T/C snv 0.020 1.000 2 2003 2017
dbSNP: rs63751287
rs63751287
13 0.742 0.120 14 73192792 missense variant A/G;T snv 0.010 1.000 1 2001 2001
dbSNP: rs63749961
rs63749961
3 0.925 0.080 14 73192772 missense variant T/G snv 0.010 1.000 1 2004 2004
dbSNP: rs63750487
rs63750487
3 0.882 0.120 14 73192771 missense variant C/T snv 0.010 1.000 1 2016 2016