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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RRM2B
(R399* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
RRM2B
(P105S)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance