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: rs73081554
rs73081554
1 1.000 0.120 3 58317208 intron variant C/T snv 4.3E-02 0.800 1.000 3 2014 2019