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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHDDS
(K21N)
Single nucleotide variant
(missense variant +1 more)
Developmental delay and seizures with or without movement abnormalities
GUncertain significance
DHDDS
(R37H)
Single nucleotide variant
(missense variant +1 more)
Retinitis pigmentosa 59
+2 more
GPathogenic/Likely pathogenic
DHDDS
(R38C)
Single nucleotide variant
(missense variant +1 more)
Retinitis pigmentosa 59
+2 more
GConflicting classifications of pathogenicity
DHDDS
(V134M +2 more)
Single nucleotide variant
(missense variant +1 more)
Developmental delay and seizures with or without movement abnormalities
+1 more
GUncertain significance
DHDDS
(R211Q +3 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 59
+2 more
GPathogenic
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