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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FSCN2
(V17I)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 30
+1 more
GLikely benign
FSCN2
Single nucleotide variant
(synonymous variant)
Retinitis pigmentosa 30
+3 more
GBenign
FSCN2
(V277I)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 30
+2 more
GConflicting classifications of pathogenicity
FSCN2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
FSCN2
(G369S +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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