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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130060040, CHRNE
Single nucleotide variant
(intron variant)
Congenital myasthenic syndrome 4B
+4 more
GBenign/Likely benign
CHRNE, LOC130060040
Microsatellite
(intron variant)
not specified
+2 more
GBenign