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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LRAT
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
LRAT
(K133T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LRAT
(A135S)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa
+3 more
GUncertain significance
LRAT
(A197fs)
Duplication
(frameshift variant)
not provided
GPathogenic
LRAT
Single nucleotide variant
(3 prime UTR variant)
Leber congenital amaurosis 14
+3 more
GUncertain significance
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