Variant (rsID / SNP)
rs34190017
rs34190017 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYT10. Location: chromosome 12, position 33,532,804. The table records no clinical significance for this variant.
Reference-table entries
SYT10Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:33532804
- HGVS
- NM_198992.4,c.1463A>C,p.His488Pro
- Allele change
- Missense_H488P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.