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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GREB1L
(V1690M)
Single nucleotide variant
(missense variant)
Renal hypodysplasia/aplasia 3
GUncertain significance
GREB1L
(T1872fs)
Duplication
(frameshift variant)
Renal hypodysplasia/aplasia 3
GUncertain significance