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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HYAL1
(R142W +3 more)
Single nucleotide variant
(missense variant +1 more)
Deficiency of hyaluronoglucosaminidase
+1 more
GUncertain significance
HYAL1
(G256R +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+3 more
GBenign/Likely benign
HYAL1
(R14fs +1 more)
Deletion
(frameshift variant +2 more)
Deficiency of hyaluronoglucosaminidase
GPathogenic/Likely pathogenic
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