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: rs1057518919
rs1057518919
5 0.851 0.120 14 73171023 missense variant T/G snv 0.010 1.000 1 2014 2014
dbSNP: rs1312532981
rs1312532981
1 1.000 0.080 14 73170846 missense variant A/G snv 0.010 1.000 1 2016 2016
dbSNP: rs1362575880
rs1362575880
4 0.851 0.120 14 73192840 missense variant A/C snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1446915570
rs1446915570
2 0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs165932
rs165932
2 0.925 0.080 14 73198145 intron variant G/A;T snv 0.61 0.010 1.000 1 2007 2007
dbSNP: rs1800839
rs1800839
1 1.000 0.080 14 73136423 5 prime UTR variant C/T snv 5.7E-02 0.010 1.000 1 2017 2017
dbSNP: rs200576075
rs200576075
2 0.925 0.080 14 73171031 missense variant C/T snv 0.010 1.000 1 2011 2011
dbSNP: rs3025786
rs3025786
1 1.000 0.080 14 73198010 non coding transcript exon variant T/C snv 3.5E-02 3.6E-02 0.010 1.000 1 2008 2008
dbSNP: rs41345849
rs41345849
1 1.000 0.080 14 73173634 missense variant C/G snv 0.010 1.000 1 2008 2008
dbSNP: rs63749885
rs63749885
3 0.882 0.080 14 73186859 missense variant C/T 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 2019 2019
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
4 0.851 0.080 14 73219188 missense variant C/T snv 0.010 1.000 1 2016 2016
dbSNP: rs63750050
rs63750050
5 0.925 0.080 14 73198106 missense variant T/G snv 0.010 1.000 1 1998 1998
dbSNP: rs63750311
rs63750311
8 0.790 0.240 14 73192647 missense variant A/C snv 0.010 1.000 1 2000 2000
dbSNP: rs63750353
rs63750353
2 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
10 0.790 0.120 14 73186860 missense variant A/G snv 0.010 1.000 1 1996 1996
dbSNP: rs63750599
rs63750599
7 0.827 0.160 14 73170963 missense variant T/C snv 0.010 1.000 1 2019 2019
dbSNP: rs63750730
rs63750730
6 0.827 0.120 14 73173574 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs63750800
rs63750800
3 0.882 0.080 14 73173585 missense variant G/A snv 0.010 1.000 1 2018 2018
dbSNP: rs63750815
rs63750815
3 0.882 0.080 14 73170974 missense variant G/T snv 0.010 1.000 1 2002 2002
dbSNP: rs63750852
rs63750852
8 0.790 0.120 14 73170998 missense variant G/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs63750886
rs63750886
5 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