Variant (rsID / SNP)
rs17860364
rs17860364 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CELA1. Location: chromosome 12, position 51,723,499. The table records no clinical significance for this variant.
Reference-table entries
CELA1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:51723499
- HGVS
- NM_001971.6,c.728A>G,p.Gln243Arg
- Allele change
- Missense_Q243R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.