Variant (rsID / SNP)
rs151335066
rs151335066 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC40. Location: chromosome 17, position 78,061,600. Clinical significance in the table: Benign.
Reference-table entries
CCDC40Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:78061600
- Cytoband
- 17q25.3
- HGVS
- NM_017950.4(CCDC40):c.2619+25G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.