Variant (rsID / SNP)
rs139150276
rs139150276 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNI3. Location: chromosome 19, position 55,668,029. Clinical significance in the table: Benign.
Reference-table entries
TNNI3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:55668029
- Cytoband
- 19q13.42
- HGVS
- NM_000363.5(TNNI3):c.109-17C>A
- Allele change
- Silent
Associated conditions / phenotypes
Hypertrophic cardiomyopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.