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: rs63750601
rs63750601
3 0.882 0.080 14 73170995 missense variant G/T snv 0.010 1.000 1 1996 1996
dbSNP: rs63751420
rs63751420
2 0.925 0.080 14 73198040 missense variant C/T snv 0.010 1.000 1 1996 1996
dbSNP: rs63751163
rs63751163
7 0.807 0.120 14 73192844 missense variant T/C snv 0.010 1.000 1 1998 1998
dbSNP: rs63749880
rs63749880
2 0.925 0.080 14 73192720 missense variant G/A snv 0.010 1.000 1 1999 1999
dbSNP: rs63750053
rs63750053
5 0.827 0.120 14 73192721 missense variant G/T snv 0.010 1.000 1 1999 1999
dbSNP: rs63751141
rs63751141
3 0.882 0.080 14 73170984 missense variant G/C snv 0.010 1.000 1 2000 2000
dbSNP: rs63751235
rs63751235
6 0.807 0.120 14 73198117 missense variant C/G snv 0.010 1.000 1 2000 2000
dbSNP: rs63751106
rs63751106
5 0.827 0.080 14 73173643 missense variant T/A;C snv 0.010 1.000 1 2001 2001
dbSNP: rs63751441
rs63751441
3 0.882 0.080 14 73173684 missense variant C/G;T snv 5.2E-05 0.010 1.000 1 2001 2001
dbSNP: rs63750311
rs63750311
8 0.790 0.240 14 73192647 missense variant A/C snv 0.010 1.000 1 2002 2002
dbSNP: rs63750634
rs63750634
3 0.925 0.120 14 73192843 missense variant T/G snv 0.010 1.000 1 2003 2003
dbSNP: rs765670175
rs765670175
7 0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 0.020 1.000 2 2005 2006
dbSNP: rs63750083
rs63750083
13 0.732 0.160 14 73219177 missense variant C/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs63750852
rs63750852
8 0.790 0.120 14 73170998 missense variant G/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs661
rs661
6 0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs63750590
rs63750590
10 0.790 0.120 14 73186860 missense variant A/G snv 0.020 1.000 2 1996 2007
dbSNP: rs121917808
rs121917808
3 0.882 0.080 14 73219192 missense variant C/A snv 0.010 1.000 1 2007 2007
dbSNP: rs63749824
rs63749824
8 0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.010 < 0.001 1 2007 2007
dbSNP: rs63751309
rs63751309
3 0.882 0.080 14 73192733 missense variant T/C snv 0.020 1.000 2 1996 2008
dbSNP: rs1179768627
rs1179768627
2 0.925 0.080 14 73198064 missense variant T/G snv 4.0E-06 0.010 < 0.001 1 2011 2011
dbSNP: rs779296437
rs779296437
2 0.925 0.080 14 73192699 missense variant A/T snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs63750306
rs63750306
17 0.701 0.320 14 73173663 missense variant A/C;G;T snv 0.090 1.000 9 1997 2013
dbSNP: rs63750301
rs63750301
6 0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs63750802
rs63750802
7 0.851 0.080 14 73219144 missense variant T/G snv 0.010 1.000 1 2013 2013
dbSNP: rs63751032
rs63751032
7 0.851 0.080 14 73219156 missense variant T/A;G snv 0.010 1.000 1 2013 2013