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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRIA3
Duplication
(5 prime UTR variant)
Inborn genetic diseases
+3 more
GBenign
GRIA3
(A133T)
Single nucleotide variant
(missense variant)
History of neurodevelopmental disorder
+2 more
GConflicting classifications of pathogenicity
GRIA3
(R216*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
GRIA3
(R394Q)
Single nucleotide variant
(missense variant)
GRIA3-related condition
+4 more
GBenign/Likely benign
GRIA3
(S567R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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