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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAGI2, LOC129998720
(R1370P +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome 15
+2 more
GUncertain significance
MAGI2, LOC129998720
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
LOC129998720, MAGI2
(G1334V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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