Variant (rsID / SNP)
rs2517449
rs2517449 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUCL3. Location: chromosome 6, position 30,919,701. The table records no clinical significance for this variant.
Reference-table entries
MUCL3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30919701
- HGVS
- NM_080870.4,c.3460T>C,p.Leu1154Leu
- Allele change
- Synonymous_L1154L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
