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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
L1CAM
(V768I +1 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia
+4 more
GConflicting classifications of pathogenicity
L1CAM
Single nucleotide variant
(synonymous variant)
Hereditary spastic paraplegia
+4 more
GBenign/Likely benign
L1CAM
(V324M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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