Variant (rsID / SNP)
rs6503905
rs6503905 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMG8. Location: chromosome 17, position 57,287,454. The table records no clinical significance for this variant.
Reference-table entries
SMG8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:57287454
- HGVS
- NM_018149.7,c.42A>G,p.Ala14Ala
- Allele change
- Synonymous_A14A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.