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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SRGAP1
(C269Y)
Single nucleotide variant
(missense variant)
Nephronophthisis
GUncertain significance
SRGAP1
(P642T +1 more)
Single nucleotide variant
(missense variant)
Congenital anomalies of kidney and urinary tract 1
GUncertain significance