Variant (rsID / SNP)
rs6843141
rs6843141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TET2. Location: chromosome 4, position 106,155,751. Clinical significance in the table: Benign.
Reference-table entries
TET2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:106155751
- Cytoband
- 4q24
- HGVS
- NM_001127208.3(TET2):c.652G>A (p.Val218Met)
- Allele change
- Missense_V218M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.