Variant (rsID / SNP)

rs397517887

rs397517887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,105,866. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

LMNALikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: Deletion
Chromosome / position: 1:156105866
Cytoband: 1q22
HGVS: NM_170707.4(LMNA):c.1111_1125del (p.Met371_Ala375del)

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.