Variant (rsID / SNP)

rs2236722

rs2236722 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP19A1. Location: chromosome 15, position 51,534,995. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CYP19A1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:51534995
Cytoband: 15q21.2
HGVS: NM_000103.4(CYP19A1):c.115T>C (p.Trp39Arg)
Allele change: Silent

Associated conditions / phenotypes

Aromatase deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.