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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATRX
(E1377G +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability-hypotonic facies syndrome, X-linked, 1
+4 more
GConflicting classifications of pathogenicity
ATRX
(G749A +1 more)
Single nucleotide variant
(missense variant)
Acquired hemoglobin H disease
+2 more
GUncertain significance
ATRX
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign/Likely benign
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