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: rs28683503
rs28683503
CEACAM5
1 1.000 0.040 19 41709863 missense variant T/C snv 0.14 0.22 0.010 1.000 1 2018 2018