Variant (rsID / SNP)
rs3760873
rs3760873 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT1. Location: chromosome 19, position 55,648,270. Clinical significance in the table: Benign.
Reference-table entries
TNNT1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:55648270
- Cytoband
- 19q13.42
- HGVS
- NM_003283.6(TNNT1):c.611+201C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.