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: rs1028344225
rs1028344225
RARB
3 0.925 0.120 3 25596566 missense variant C/T snv 0.020 1.000 2 2013 2016