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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPRED1
(V17A)
Single nucleotide variant
(missense variant)
Legius syndrome
+1 more
GUncertain significance
SPRED1
(A142S)
Single nucleotide variant
(missense variant)
Legius syndrome
GUncertain significance
SPRED1
(N182K)
Single nucleotide variant
(missense variant)
Legius syndrome
GUncertain significance
SPRED1
(M425V)
Single nucleotide variant
(missense variant)
Legius syndrome
+1 more
GUncertain significance
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