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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INVS
(L206S +2 more)
Single nucleotide variant
(missense variant +1 more)
Nephronophthisis
+1 more
GUncertain significance
INVS
(R899* +2 more)
Single nucleotide variant
(nonsense +1 more)
Nephronophthisis
+2 more
GPathogenic
INVS
(H941R +2 more)
Single nucleotide variant
(missense variant +1 more)
Infantile nephronophthisis
+2 more
GUncertain significance
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