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: rs7902091
rs7902091
CTNNA3
2 1.000 0.040 10 66838534 intron variant C/A snv 0.29 0.710 1.000 1 2014 2014