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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SFXN4
(A226V)
Single nucleotide variant
(missense variant +1 more)
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
+1 more
GConflicting classifications of pathogenicity
SFXN4
(L123*)
Single nucleotide variant
(nonsense +1 more)
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
GPathogenic