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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EDN3
(T189fs)
Duplication
EDN3-related disorder
+4 more
GBenign/Likely benign
EDN3
(A224T +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+2 more
GLikely benign