Variant (rsID / SNP)
rs9666607
rs9666607 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD44. Location: chromosome 11, position 35,226,155. The table records no clinical significance for this variant.
Reference-table entries
CD44Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:35226155
- HGVS
- NM_000610.4,c.1250A>G,p.Lys417Arg
- Allele change
- Silent
Associated conditions / phenotypes
Systemic Lupus Erythematosus|Autoimmune Disease|Lupus Erythematosus|Prostate Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.