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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP19A1, MIR4713HG
+1 more
Single nucleotide variant
(3 prime UTR variant)
Aromatase excess syndrome
+2 more
GBenign
CYP19A1, MIR4713HG
+1 more
Single nucleotide variant
(synonymous variant)
Aromatase deficiency
+2 more
GBenign