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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDE6B
(P41fs)
Deletion
(frameshift variant)
Autosomal recessive retinitis pigmentosa
GPathogenic
PDE6B, PDE6B-AS1
(C270*)
Single nucleotide variant
(nonsense +1 more)
See cases
+3 more
GPathogenic
PDE6B, PDE6B-AS1
Single nucleotide variant
(splice donor variant)
Retinitis pigmentosa 40
+2 more
GPathogenic/Likely pathogenic
PDE6B
(H337R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely pathogenic
PDE6B
(W807R +2 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 40
+1 more
GPathogenic
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