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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FRMD7
(L277P +1 more)
Single nucleotide variant
(missense variant)
Nystagmus 1, congenital, X-linked
+1 more
GConflicting classifications of pathogenicity
FRMD7
Single nucleotide variant
(synonymous variant)
Nystagmus 1, congenital, X-linked
GUncertain significance