Variant (rsID / SNP)
rs1106569
rs1106569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFB2. Location: chromosome 1, position 218,520,587. Clinical significance in the table: Likely benign.
Reference-table entries
TGFB2Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:218520587
- Cytoband
- 1q41
- HGVS
- NM_003238.6(TGFB2):c.346+198T>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.