Variant (rsID / SNP)

rs36044314

rs36044314 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA2. Location: chromosome 6, position 129,571,272. 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: 6:129571272
Cytoband: 6q22.33
HGVS: NM_000426.4(LAMA2):c.1798G>A (p.Gly600Arg)
Allele change: Missense_G600R

Associated conditions / phenotypes

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

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.