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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CARD14
(E138K)
Single nucleotide variant
(missense variant +1 more)
not provided
GPathogenic
CARD14, SGSH
(R245H)
Single nucleotide variant
(missense variant +1 more)
SGSH-related condition
+4 more
GPathogenic