Variant (rsID / SNP)
rs550404
rs550404 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYTL2. Location: chromosome 11, position 85,435,730. The table records no clinical significance for this variant.
Reference-table entries
SYTL2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:85435730
- HGVS
- NM_206927.4,c.4671G>A,p.Pro1557Pro
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.