Variant (rsID / SNP)

rs201227908

rs201227908 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,104,659. Clinical significance in the table: Uncertain significance.

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Reference-table entries

LMNAUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:156104659
Cytoband: 1q22
HGVS: NM_170707.4(LMNA):c.703C>A (p.Arg235Ser)
Allele change: Missense_R235C

Associated conditions / phenotypes

Congenital muscular dystrophy due to LMNA mutation

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.