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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP4V2, DBET
+67 more
Deletion
Hereditary factor XI deficiency disease
GLikely pathogenic
DUX4
(V318D)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance