Variant (rsID / SNP)
rs6141
rs6141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THPO. Location: chromosome 3, position 184,090,266. Clinical significance in the table: Benign.
Reference-table entries
THPOBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:184090266
- Cytoband
- 3q27.1
- HGVS
- NM_000460.4(THPO):c.*35G>A
- Allele change
- Silent
Associated conditions / phenotypes
Thrombocythemia 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.