rs878854368, NEB

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.
Nemaline Myopathy 2
CUI: C1850569
Disease: Nemaline Myopathy 2
265 1.000 0.080 2 151646140 frameshift variant GATT/- delins 7.0E-06 0.700 1.000 3 2006 2016