Variant (rsID / SNP)
rs59267781
rs59267781 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,108,448. The table records no clinical significance for this variant.
Reference-table entries
LMNANot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:156108448
- Cytoband
- 1q22
- HGVS
- NM_170707.4(LMNA):c.1868C>G (p.Thr623Ser)
- Allele change
- Silent
Associated conditions / phenotypes
Hutchinson-Gilford syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.