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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLX4
(V1641fs)
Duplication
(frameshift variant)
Fanconi anemia complementation group P
+1 more
GConflicting classifications of pathogenicity
SLX4
(E36*)
Single nucleotide variant
(nonsense)
Fanconi anemia
+1 more
GPathogenic/Likely pathogenic