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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
XRCC2
(S205A)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group U
+3 more
GConflicting classifications of pathogenicity
XRCC2
(I43N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance