Variant (rsID / SNP)
rs2457829
rs2457829 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to L1TD1. Location: chromosome 1, position 62,672,546. The table records no clinical significance for this variant.
Reference-table entries
L1TD1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:62672546
- HGVS
- NM_001164835.2,c.246G>A,p.Gly82Gly
- Allele change
- Synonymous_G82G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
