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: rs387906737
rs387906737
DLX5
1 1.000 0.200 7 97022192 missense variant T/G snv 0.800 1.000 1 2012 2012