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: rs137852883
rs137852883
CLN8
1 1.000 0.120 8 1771142 missense variant G/A;C;T snv 4.0E-06; 2.4E-05 0.800 1.000 7 2004 2016