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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCA4
(T681I)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
SMARCA4
(M1233R)
Single nucleotide variant
(missense variant +1 more)
Microcephaly
GUncertain significance