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: rs28934002
rs28934002
ATP1A2
1 1.000 1 160128767 missense variant C/A;T snv 0.800 1.000 1 2004 2004