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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCG2, ABRAXAS1
+338 more
Copy number loss
Chromosome 4q21 deletion syndrome
GPathogenic
PKD2
(M800L)
Single nucleotide variant
(missense variant +1 more)
Joubert syndrome 7
+4 more
GConflicting classifications of pathogenicity