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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SFXN4
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GBenign
SFXN4
Single nucleotide variant
(intron variant)
Growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome
+2 more
GBenign
SFXN4
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
SFXN4
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
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