Variant (rsID / SNP)

rs373721390

rs373721390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,084,787. 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: 1:156084787
Cytoband: 1q22
HGVS: NM_170707.4(LMNA):c.78C>T (p.Ile26=)
Allele change: Synonymous_I26I

Associated conditions / phenotypes

Charcot-Marie-Tooth disease type 2|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.