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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSTB
Single nucleotide variant
(splice acceptor variant)
Microcephaly
+6 more
GPathogenic
CSTB, LOC130066788
Single nucleotide variant
(synonymous variant)
Progressive myoclonic epilepsy
+4 more
GBenign/Likely benign