Variant (rsID / SNP)
rs61235244
rs61235244 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,106,215. Clinical significance in the table: Pathogenic.
Reference-table entries
LMNAPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:156106215
- Cytoband
- 1q22
- HGVS
- NM_170707.4(LMNA):c.1368C>A (p.Asn456Lys)
- Allele change
- Missense_N456K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.