Variant (rsID / SNP)
rs2046210
rs2046210 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC170. Location: chromosome 6, position 151,948,366. Clinical significance in the table: Benign.
Reference-table entries
CCDC170Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:151948366
- Cytoband
- 6q25.1
- HGVS
- NC_000006.12:g.151627231G>A
Associated conditions / phenotypes
Estrogen resistance syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.