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: rs587777134
rs587777134
CTNNA3
1 1.000 10 67606868 missense variant A/T snv 0.800 1.000 1 2013 2013
dbSNP: rs587777135
rs587777135
CTNNA3
2 0.925 0.080 10 65966714 inframe deletion CAA/- delins 0.700 0