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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HNF1B
(G438S +1 more)
Single nucleotide variant
(missense variant +1 more)
Renal cysts and diabetes syndrome
+4 more
GUncertain significance
AATF, ACACA
+15 more
Copy number loss
Chromosome 17q12 deletion syndrome
GPathogenic
AATF, ACACA
+22 more
Copy number loss
Chromosome 17q12 deletion syndrome
GPathogenic
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