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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HTRA2
(E281V +2 more)
Single nucleotide variant
(missense variant +1 more)
Leigh syndrome
GUncertain significance
HTRA2, LOXL3
(V391E)
Single nucleotide variant
(3 prime UTR variant +3 more)
Leigh syndrome
GUncertain significance