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: rs1566630910
rs1566630910
1 1.000 0.080 14 73173651 missense variant G/A snv 0.700 0
dbSNP: rs1566638673
rs1566638673
1 1.000 0.080 14 73186881 inframe insertion -/TAT delins 0.700 0
dbSNP: rs1566656702
rs1566656702
1 1.000 0.080 14 73217173 missense variant G/T snv 0.700 0
dbSNP: rs1566657804
rs1566657804
1 1.000 0.080 14 73219182 missense variant C/T snv 0.700 0
dbSNP: rs63750009
rs63750009
5 0.851 0.120 14 73192760 missense variant A/C;G snv 0.700 0
dbSNP: rs63750219
rs63750219
1 1.000 0.080 14 73206385 splice acceptor variant G/A;T snv 0.700 0
dbSNP: rs63750231
rs63750231
23 0.689 0.160 14 73198100 missense variant A/C;G snv 0.100 0.955 22 1997 2020
dbSNP: rs63750306
rs63750306
17 0.701 0.320 14 73173663 missense variant A/C;G;T snv 0.100 1.000 10 2001 2017
dbSNP: rs17125721
rs17125721
14 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 0.090 1.000 9 1998 2019
dbSNP: rs63750526
rs63750526
10 0.776 0.160 14 73192832 missense variant C/A snv 0.070 1.000 7 2000 2014
dbSNP: rs765670175
rs765670175
7 0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 0.060 1.000 6 1997 2010
dbSNP: rs63750265
rs63750265
3 0.882 0.080 14 73186869 missense variant T/A;C;G snv 0.040 1.000 4 2002 2016
dbSNP: rs63750301
rs63750301
6 0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 0.040 1.000 4 2002 2014
dbSNP: rs63749824
rs63749824
8 0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.030 1.000 3 2016 2016
dbSNP: rs63750004
rs63750004
4 0.851 0.080 14 73173655 missense variant T/A;C snv 0.030 1.000 3 1999 2010
dbSNP: rs63750082
rs63750082
13 0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 0.030 1.000 3 2001 2019
dbSNP: rs63750083
rs63750083
13 0.732 0.160 14 73219177 missense variant C/A;T snv 0.030 1.000 3 2002 2019
dbSNP: rs63749805
rs63749805
6 0.807 0.120 14 73173577 missense variant C/G;T snv 0.020 1.000 2 1998 2018
dbSNP: rs63750391
rs63750391
3 0.882 0.160 14 73173665 missense variant G/A;C;T snv 0.020 1.000 2 1996 2016
dbSNP: rs63750577
rs63750577
8 0.827 0.120 14 73186881 missense variant C/T snv 0.020 1.000 2 2005 2007
dbSNP: rs63750646
rs63750646
6 0.807 0.120 14 73217147 missense variant G/C snv 0.020 1.000 2 1999 1999
dbSNP: rs63750929
rs63750929
4 0.882 0.080 14 73217177 missense variant G/T snv 0.020 0.500 2 2008 2020
dbSNP: rs63751163
rs63751163
7 0.807 0.120 14 73192844 missense variant T/C snv 0.020 1.000 2 1998 2000
dbSNP: rs661
rs661
6 0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 0.020 1.000 2 2007 2007
dbSNP: rs1057518919
rs1057518919
5 0.851 0.120 14 73171023 missense variant T/G snv 0.010 1.000 1 2014 2014