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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA1
Single nucleotide variant
(synonymous variant)
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
+1 more
GConflicting classifications of pathogenicity
LAMA1
Single nucleotide variant
(synonymous variant)
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
+2 more
GLikely benign
LAMA1
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LAMA1, LOC112543434
Single nucleotide variant
(intron variant)
not provided
GBenign
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