NEB, nebulin, 4703

N. diseases: 148; N. variants: 280
Disease: Nemaline Myopathy 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057516676
rs1057516676
Entrez Id: 4703
Gene Symbol: NEB
NEB
CUI: C1850569
Disease:
Nemaline Myopathy 2 		A 0.700 GeneticVariation CLINVAR