Variant (rsID / SNP)
rs9390459
rs9390459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STXBP5. Location: chromosome 6, position 147,680,359. The table records no clinical significance for this variant.
Reference-table entries
STXBP5Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:147680359
- HGVS
- NM_001127715.4,c.2445A>G,p.Leu815Leu
- Allele change
- Synonymous_L779L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.