Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62636522
rs62636522
Entrez Id: 4747
Gene Symbol: NEFL
NEFL
CUI: C0007959
Disease:
Charcot-Marie-Tooth Disease
0.010 GeneticVariation BEFREE Furthermore, the sibling of one of the patients was also affected with CMT but did not have the I214M substitution. 16930284 2006