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: rs11209026
rs11209026
5 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 1.000 3 2007 2020
dbSNP: rs10889677
rs10889677
2 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.820 1.000 1 2009 2020
dbSNP: rs2201841
rs2201841
3 0.716 0.440 1 67228519 intron variant A/G;T snv 0.820 1.000 1 2010 2017
dbSNP: rs7517847
rs7517847
5 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.730 1.000 1 2008 2016
dbSNP: rs76418789
rs76418789
2 0.882 0.080 1 67182913 missense variant G/A snv 7.3E-03 4.5E-03 0.710 1.000 1 2016 2016
dbSNP: rs80174646
rs80174646
5 0.827 0.120 1 67242472 intron variant G/T snv 5.8E-02 0.700 1.000 2 2015 2016
dbSNP: rs10889676
rs10889676
5 0.827 0.120 1 67256884 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11580078
rs11580078
14 0.724 0.240 1 67203951 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs11581607
rs11581607
4 0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs183686347
rs183686347
5 0.827 0.120 1 67237759 intron variant G/A snv 4.8E-03 0.700 1.000 1 2016 2016