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Variant (rsID / SNP)

rs111381107

LAMA2

rs111381107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA2. Location: chromosome 6, position 129,513,917. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

LAMA2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
6:129513917
Cytoband
6q22.33
HGVS
NM_000426.4(LAMA2):c.1701C>T (p.Ile567=)
Allele change
Synonymous_I567I

Associated conditions / phenotypes

Congenital muscular dystrophy due to partial LAMA2 deficiency|LAMA2-related muscular dystrophy

Public references

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