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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HARS2
Single nucleotide variant
(synonymous variant +1 more)
Perrault syndrome 2
+2 more
GBenign/Likely benign
HARS2
(G369R +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign