Variant (rsID / SNP)
rs2616815
rs2616815 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DCDC1. Location: chromosome 11, position 31,327,316. The table records no clinical significance for this variant.
Reference-table entries
DCDC1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:31327316
- HGVS
- NM_001387274.1,c.600G>A,p.Glu200Glu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.