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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PAX6_HS3, PAX6_HS8
+334 more
Copy number loss
See cases
GPathogenic
LOC130005444, FANCF
(V295I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign