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Variant (rsID / SNP)

rs58672172

LMNA

rs58672172 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,106,042. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LMNAConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:156106042
Cytoband
1q22
HGVS
NM_170707.4(LMNA):c.1195C>T (p.Arg399Cys)
Allele change
Missense_R399C

Associated conditions / phenotypes

Familial partial lipodystrophy, Dunnigan type|Charcot-Marie-Tooth disease type 2|Cardiomyopathy|Charcot-Marie-Tooth disease|Primary dilated cardiomyopathy

Public references

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