Variant (rsID / SNP)
rs1800471
rs1800471 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFB1. Location: chromosome 19, position 41,858,876. Clinical significance in the table: Benign.
Reference-table entries
TGFB1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:41858876
- Cytoband
- 19q13.2
- HGVS
- NM_000660.7(TGFB1):c.74G>C (p.Arg25Pro)
- Allele change
- Missense_R25P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.