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: rs74315390
rs74315390
8 0.790 0.120 20 63439609 missense variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs796052621
rs796052621
6 0.827 0.080 20 63444756 missense variant C/T snv 0.010 1.000 1 2017 2017