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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FANCF, LOC130005443
(P318S)
Single nucleotide variant
(missense variant)
Fanconi anemia
+1 more
GUncertain significance
FANCF
(V31M)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance