Variant (rsID / SNP)
rs80356814
rs80356814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,108,488. The table records no clinical significance for this variant.
Reference-table entries
LMNANot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:156108488
- Cytoband
- 1q22
- HGVS
- NM_170707.4(LMNA):c.1908C>T (p.Ser636=)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.