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: rs882083
rs882083
CCDC26
1 1.000 0.080 8 128970510 intron variant C/T snv 0.41 0.700 1.000 3 2009 2012