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: rs4986790
rs4986790
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs4986791
rs4986791
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs5743708
rs5743708
98 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 0.020 1.000 2 2006 2011
dbSNP: rs28940578
rs28940578
16 0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 0.020 1.000 2 2014 2017
dbSNP: rs61752717
rs61752717
72 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 0.030 0.667 3 2004 2017
dbSNP: rs104895105
rs104895105
7 0.851 0.120 16 3247171 missense variant G/A snv 0.010 1.000 1 2004 2004
dbSNP: rs224222
rs224222
15 0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 0.010 1.000 1 2016 2016
dbSNP: rs756465037
rs756465037
LTF
6 0.807 0.200 3 46439392 missense variant C/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs104895224
rs104895224
3 0.882 0.080 12 6333808 missense variant C/G;T snv 0.010 1.000 1 2001 2001
dbSNP: rs104895218
rs104895218
5 0.827 0.240 12 6334099 missense variant C/T snv 0.010 1.000 1 2004 2004