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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FANCF
(G118V)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group F
GUncertain significance
FANCF
(A81S)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity