Variant (rsID / SNP)
rs16826617
rs16826617 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIT1. Location: chromosome 1, position 40,310,221. Clinical significance in the table: Benign.
Reference-table entries
TRIT1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:40310221
- Cytoband
- 1p34.2
- HGVS
- NM_017646.6(TRIT1):c.1098C>T (p.Ile366=)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.