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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NKX2-2
(S99L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NKX2-2
(N36K)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
NKX2-2
(P32L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
NKX2-2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
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