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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HARS1
Deletion
(inframe_deletion)
not provided
+2 more
GUncertain significance
HARS1
(R232C +6 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity