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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PARN
(D383N +2 more)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita, autosomal recessive 6
GUncertain significance
PARN
(A156S +2 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity