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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMB2
(T1635fs)
Microsatellite
(frameshift variant)
LAMB2-related infantile-onset nephrotic syndrome
GPathogenic
LAMB2
Deletion
(frameshift variant)
Pierson syndrome
GLikely pathogenic
LAMB2
(R58Q)
Single nucleotide variant
(missense variant)
LAMB2-related infantile-onset nephrotic syndrome
+1 more
GUncertain significance
LAMB2
(R44fs)
Deletion
(frameshift variant)
Pierson syndrome
GLikely pathogenic
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