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: rs2302188
rs2302188
CEACAM21
1 1.000 0.120 19 41579520 missense variant G/A snv 0.36 0.010 < 0.001 1 2009 2009