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: rs1394871648
rs1394871648
ALS2
1 1.000 2 201761816 missense variant C/T snv 4.1E-06 0.010 1.000 1 2009 2009