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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EBP
(R147H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
EBP
(W186R)
Single nucleotide variant
(missense variant)
MEND syndrome
+1 more
GUncertain significance