Variant (rsID / SNP)
rs4646
rs4646 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP19A1. Location: chromosome 15, position 51,502,844. Clinical significance in the table: Benign.
Reference-table entries
CYP19A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:51502844
- Cytoband
- 15q21.2
- HGVS
- NM_000103.4(CYP19A1):c.*161T>G
- Allele change
- Silent
Associated conditions / phenotypes
Aromatase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.