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: 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: rs11580078
rs11580078
14 0.724 0.240 1 67203951 intron variant C/A;G snv 0.700 1.000 1 2015 2015