Variant (rsID / SNP)
rs1063280
rs1063280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM15. Location: chromosome 6, position 30,140,342. The table records no clinical significance for this variant.
Reference-table entries
TRIM15Not classified
- Variant type
- 3_prime_UTR_variant
- Chromosome / position
- 6:30140342
- HGVS
- NM_033229.3,c.*216T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.