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Variant (rsID / SNP)

rs372011095

LMNA

rs372011095 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,106,223. 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
1:156106223
Cytoband
1q22
HGVS
NM_170707.4(LMNA):c.1376A>G (p.Asn459Ser)
Allele change
Missense_N459S

Associated conditions / phenotypes

Charcot-Marie-Tooth disease type 2|Cardiomyopathy

Public references

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