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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLX4
Single nucleotide variant
(3 prime UTR variant)
Fanconi anemia complementation group P
GConflicting classifications of pathogenicity
SLX4
(E1540K)
Single nucleotide variant
(missense variant)
Fanconi anemia
+1 more
GConflicting classifications of pathogenicity