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: rs864309524
rs864309524
HOMER2
1 1.000 15 82854741 missense variant C/G;T snv 4.0E-06 0.800 1.000 1 2015 2015