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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AFF2
(L610F +5 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
AFF2
(P886A +5 more)
Single nucleotide variant
(missense variant)
AFF2-related disorder
+3 more
GBenign/Likely benign
AFF2
(R927H +5 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GLikely benign
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