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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HARS1
(T482M +6 more)
Single nucleotide variant
(missense variant)
Usher syndrome type 3B
+2 more
GConflicting classifications of pathogenicity
HARS1
(V326M +6 more)
Single nucleotide variant
(missense variant)
Charcot-Marie-Tooth disease
+3 more
GUncertain significance