Variant (rsID / SNP)
rs59673
rs59673 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC162P. Location: chromosome 6, position 109,548,713. The table records no clinical significance for this variant.
Reference-table entries
CCDC162PNot classified
- Variant type
- non_coding_transcript_exon_variant
- Chromosome / position
- 6:109548713
- HGVS
- NR_152435.1,n.1756C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.