Variant (rsID / SNP)
rs1050922
rs1050922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD6. Location: chromosome 11, position 60,785,352. The table records no clinical significance for this variant.
Reference-table entries
CD6Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:60785352
- HGVS
- NM_006725.5,c.1704A>G,p.Ser568Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
