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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130004599, NFKB2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC130004599, NFKB2
(P430S +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity