Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768892432
rs768892432
Entrez Id: 285489;105374355
Gene Symbol: DOK7;LOC105374355
DOK7;LOC105374355
CUI: C1850792
Disease:
Congenital myasthenic syndrome ib
0.700 GeneticVariation UNIPROT