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: rs10997691
rs10997691
CTNNA3
1 1.000 0.080 10 67521827 intron variant A/C snv 0.16 0.13 0.010 < 0.001 1 2016 2016