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: rs1057518767
rs1057518767
5 0.851 0.120 1 94098874 missense variant A/T snv 0.700 0
dbSNP: rs398123339
rs398123339
5 0.851 0.120 1 94113068 splice acceptor variant T/C snv 4.0E-06 0.700 0