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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATRX
(F2015V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ATRX
(Y228H +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability-hypotonic facies syndrome, X-linked, 1
GUncertain significance
ATRX
(N179S +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
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