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 2008 2018
dbSNP: rs7517847
rs7517847
5 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.720 1.000 1 2012 2018
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: rs183686347
rs183686347
5 0.827 0.120 1 67237759 intron variant G/A snv 4.8E-03 0.700 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 1 2016 2016