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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMA5
(Q2827fs)
Duplication
(frameshift variant)
Nephrotic syndrome, IIa 26
GLikely pathogenic
LAMA5
(D122N)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, IIa 26
GUncertain significance