Variant (rsID / SNP)
rs9471809
rs9471809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPS10. Location: chromosome 6, position 42,185,564. The table records no clinical significance for this variant.
Reference-table entries
MRPS10Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:42185564
- HGVS
- NM_018141.4,c.24T>G,p.Gly8Gly
- Allele change
- Synonymous_G8G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
