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: rs587783451
rs587783451
CHD7
1 1.000 0.080 8 60853012 missense variant A/G snv 0.800 1.000 15 2004 2015