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Variant (rsID / SNP)

rs267607543

LMNA

rs267607543 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,106,824. The table records no clinical significance for this variant.

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Reference-table entries

LMNANot classified
Variant type
single nucleotide variant
Chromosome / position
1:156106824
Cytoband
1q22
HGVS
NM_170707.4(LMNA):c.1488+5G>A
Allele change
Silent

Public references

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