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: rs63749961
rs63749961
3 0.925 0.080 14 73192772 missense variant T/G snv 0.010 1.000 1 2019 2019
dbSNP: rs63750001
rs63750001
3 0.851 0.080 14 73219188 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs63750050
rs63750050
4 0.925 0.080 14 73198106 missense variant T/G snv 0.010 1.000 1 1998 1998
dbSNP: rs63750311
rs63750311
7 0.790 0.240 14 73192647 missense variant A/C snv 0.010 1.000 1 2000 2000
dbSNP: rs63750353
rs63750353
1 0.925 0.080 14 73173630 missense variant A/G;T snv 0.010 1.000 1 1997 1997
dbSNP: rs63750444
rs63750444
4 0.882 0.080 14 73192745 missense variant G/A snv 0.010 1.000 1 2019 2019
dbSNP: rs63750590
rs63750590
6 0.790 0.120 14 73186860 missense variant A/G snv 0.010 1.000 1 1996 1996
dbSNP: rs63750599
rs63750599
5 0.827 0.160 14 73170963 missense variant T/C snv 0.010 1.000 1 2019 2019
dbSNP: rs63750730
rs63750730
5 0.827 0.120 14 73173574 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs63750800
rs63750800
2 0.882 0.080 14 73173585 missense variant G/A snv 0.010 1.000 1 2018 2018
dbSNP: rs63750815
rs63750815
2 0.882 0.080 14 73170974 missense variant G/T snv 0.010 1.000 1 2002 2002
dbSNP: rs63750852
rs63750852
7 0.790 0.120 14 73170998 missense variant G/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs63750886
rs63750886
2 0.851 0.080 14 73198072 missense variant C/G 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: rs63750907
rs63750907
5 0.807 0.120 14 73173667 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs63751024
rs63751024
3 0.851 0.120 14 73192793 missense variant T/C snv 0.010 1.000 1 2015 2015
dbSNP: rs63751037
rs63751037
6 0.790 0.080 14 73173642 missense variant A/G snv 0.010 1.000 1 2003 2003
dbSNP: rs63751071
rs63751071
1 1.000 0.080 14 73173656 missense variant T/G snv 0.010 1.000 1 2004 2004
dbSNP: rs63751106
rs63751106
4 0.827 0.080 14 73173643 missense variant T/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs63751141
rs63751141
2 0.882 0.080 14 73170984 missense variant G/C snv 0.010 1.000 1 2000 2000
dbSNP: rs63751223
rs63751223
1 0.807 0.160 14 73219161 missense variant G/C snv 0.010 1.000 1 2007 2007
dbSNP: rs63751254
rs63751254
3 0.851 0.160 14 73217210 missense variant A/G snv 0.010 1.000 1 2000 2000
dbSNP: rs63751287
rs63751287
10 0.742 0.120 14 73192792 missense variant A/G;T snv 0.010 1.000 1 2017 2017
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: rs866914724
rs866914724
3 0.882 0.080 14 73173685 missense variant T/C snv 0.010 1.000 1 2016 2016