Variant (rsID / SNP)
rs7941327
rs7941327 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIAE. Location: chromosome 11, position 124,506,967. The table records no clinical significance for this variant.
Reference-table entries
SIAENot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:124506967
- HGVS
- NM_170601.5,c.1452G>A,p.Thr484Thr
- Allele change
- Synonymous_T484T
Associated conditions / phenotypes
Autoimmune Disease|Rheumatoid Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
