Variant (rsID / SNP)

rs730882262

rs730882262 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,105,084. Clinical significance in the table: Pathogenic.

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Reference-table entries

LMNAPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:156105084
Cytoband: 1q22
HGVS: NM_170707.4(LMNA):c.917T>G (p.Leu306Arg)
Allele change: Missense_L306P

Associated conditions / phenotypes

Hutchinson-Gilford progeria syndrome, childhood-onset|Right ventricular cardiomyopathy

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.