rs1411928276, DCT

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 13 94479251 missense variant C/T snv 0.010 1.000 1 2019 2019