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: rs1565909334
rs1565909334
CUX2 ; LOC105369983
1 1.000 12 111310550 missense variant G/A snv 0.700 1.000 4 2012 2018