Variant (rsID / SNP)
rs6061043
rs6061043 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTLL9. Location: chromosome 20, position 30,527,065. The table records no clinical significance for this variant.
Reference-table entries
TTLL9Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:30527065
- HGVS
- NM_001008409.5,c.1239T>C,p.His413His
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.