Variant (rsID / SNP)
rs2066474
rs2066474 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HSD17B3. Location: chromosome 9, position 99,064,425. Clinical significance in the table: Benign.
Reference-table entries
HSD17B3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:99064425
- Cytoband
- 9q22.32
- HGVS
- NM_000197.2(HSD17B3):c.-39A>G
- Allele change
- Silent
Associated conditions / phenotypes
Testosterone 17-beta-dehydrogenase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.