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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MIR4713HG, CYP19A1
+1 more
(R365Q)
Single nucleotide variant
(missense variant)
Aromatase deficiency
GLikely pathogenic
PIRC66, MIR4713HG
+1 more
Single nucleotide variant
(intron variant)
Aromatase deficiency
GUncertain significance