Variant (rsID / SNP)

rs797044485

rs797044485 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,104,623. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LMNANot classified

Variant type: single nucleotide variant
Chromosome / position: 1:156104623
Cytoband: 1q22
HGVS: NM_170707.4(LMNA):c.667G>A (p.Glu223Lys)
Allele change: Missense_E223K

Associated conditions / phenotypes

Hutchinson-Gilford syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.