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Variant (rsID / SNP)

rs191899712

LAMA2

rs191899712 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA2. Location: chromosome 6, position 129,371,099. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LAMA2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
6:129371099
Cytoband
6q22.33
HGVS
NM_000426.4(LAMA2):c.149C>T (p.Ala50Val)
Allele change
Missense_A50V

Associated conditions / phenotypes

LAMA2-related muscular dystrophy|Merosin deficient congenital muscular dystrophy

Public references

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