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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FRMD7
(L277P +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FRMD7
(E268D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FRMD7
(S281L +1 more)
Single nucleotide variant
(missense variant)
Nystagmus 1, congenital, X-linked
+2 more
GBenign
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