Gene Mutations
 
Records Return:  (2) Show
 
GeneGene Omim NumberDisease Omim NumberChromosome LocationGene MutationAllelic VariantOmim PhenotypeSample Count
PMP2260109711822017p11.2DUP (17p)0001CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A5
PMP2260109714590017p11.2HIS12ARG DEJERINE-SOTTAS SYNDROME1