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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACD
(P402T +1 more)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita, autosomal dominant 6
+1 more
GUncertain significance
ACD
(K84del +1 more)
Deletion
(inframe_deletion)
Dyskeratosis congenita, autosomal dominant 6
GPathogenic