Variant (rsID / SNP)
rs2074474
rs2074474 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM39. Location: chromosome 6, position 30,309,508. The table records no clinical significance for this variant.
Reference-table entries
TRIM39Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30309508
- HGVS
- NM_021253.4,c.1029T>C,p.Pro343Pro
- Allele change
- Synonymous_P343P
Associated conditions / phenotypes
Autoimmune Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.