rs1273559032, ACTA1

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.
Myopathies, Nemaline
CUI: C0206157
Disease: Myopathies, Nemaline
42 1.000 0.080 1 229432619 missense variant C/T snv 0.010 1.000 1 2004 2004