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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATRX
(T2091A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ATRX
(Y1847F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
ATRX
(H865Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GBenign
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