Variant (rsID / SNP)
rs2057727
rs2057727 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM39. Location: chromosome 6, position 30,297,529. The table records no clinical significance for this variant.
Reference-table entries
TRIM39Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30297529
- HGVS
- NM_021253.4,c.435T>C,p.Asp145Asp
- Allele change
- Synonymous_D145D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.