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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC121627832, TCF4
(T323fs +13 more)
Duplication
(frameshift variant)
not provided
GPathogenic
LOC121627832, TCF4
(G452R +13 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity