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: rs397518483
rs397518483
RARB
9 0.851 0.120 3 25596428 missense variant C/A;T snv 0.010 1.000 1 2019 2019