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: rs398123009
rs398123009
19 0.790 0.200 11 66211206 missense variant C/T snv 7.0E-06 0.010 1.000 1 2017 2017