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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP164
(G215del)
Deletion
(inframe_deletion)
Nephronophthisis 15
GUncertain significance
CEP164
(P1302S +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
CEP164
(Q1410* +1 more)
Single nucleotide variant
(nonsense)
not specified
+3 more
GConflicting classifications of pathogenicity
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