Source: ALL
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: rs587777669
rs587777669
HNRNPDL
1 1.000 0.120 4 82426523 missense variant C/G;T snv 0.800 1.000 1 2014 2014
dbSNP: rs1553900864
rs1553900864
HNRNPDL
1 1.000 0.120 4 82427199 missense variant G/A snv 0.700 0