Variant (rsID / SNP)

rs397517911

rs397517911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,105,030. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

LMNALikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:156105030
Cytoband: 1q22
HGVS: NM_170707.4(LMNA):c.863C>G (p.Ala288Gly)
Allele change: Missense_A288G

Associated conditions / phenotypes

Primary dilated 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.