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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NKX2-5
Single nucleotide variant
(3 prime UTR variant +1 more)
Cardiovascular phenotype
+2 more
GBenign
NKX2-5
Single nucleotide variant
(3 prime UTR variant +1 more)
Cardiovascular phenotype
+3 more
GBenign
NKX2-5
Single nucleotide variant
(3 prime UTR variant +1 more)
Lissencephaly due to TUBA1A mutation
+4 more
GBenign/Likely benign
NKX2-5
Deletion
(intron variant)
not specified
GBenign
NKX2-5
Deletion
(intron variant)
not provided
GLikely benign
NKX2-5
Single nucleotide variant
(synonymous variant)
Atrial septal defect 7
+2 more
GBenign
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