Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553259566
rs1553259566
MPZ
CGCCT 0.700 CausalMutation CLINVAR A small direct tandem duplication of the myelin protein zero gene in a patient with Dejerine-Sottas disease phenotype. 9588852

1998
dbSNP: rs1553259566
rs1553259566
MPZ
CGCCT 0.700 CausalMutation CLINVAR Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype. 7530550

1994