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: rs119465999
rs119465999
UTP4
1 1.000 0.080 16 69165386 missense variant C/A;T snv 8.0E-06; 3.3E-03 0.020 1.000 2 2002 2013