Variant (rsID / SNP)
rs17860317
rs17860317 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CELA1. Location: chromosome 12, position 51,733,734. The table records no clinical significance for this variant.
Reference-table entries
CELA1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:51733734
- HGVS
- NM_001971.6,c.519C>T,p.Tyr173Tyr
- Allele change
- Synonymous_Y173Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.