| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CYP19A1, MIR4713HG
+1 more (P326S) | Single nucleotide variant (missense variant) | Aromatase deficiency +2 more | |
| | CYP19A1, MIR4713HG
+1 more | Single nucleotide variant (synonymous variant) | CYP19A1-related condition +1 more | |
| | CYP19A1, MIR4713HG
+1 more | Single nucleotide variant (synonymous variant) | CYP19A1-related condition +2 more | |
| | CYP19A1, MIR4713HG
+1 more (V17M) | Single nucleotide variant (missense variant) | Aromatase deficiency +2 more | GConflicting classifications of pathogenicity |
| | CYP19A1, LOC110386951
+2 more | Single nucleotide variant (synonymous variant) | CYP19A1-related condition +2 more | |
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