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: rs10956453
rs10956453
CCDC26
1 1.000 0.080 8 128937545 intron variant G/C snv 0.72 0.700 1.000 1 2009 2009