Variant (rsID / SNP)

rs117096733

rs117096733 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA2. Location: chromosome 6, position 129,618,791. Clinical significance in the table: Likely benign.

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Reference-table entries

LAMA2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:129618791
Cytoband: 6q22.33
HGVS: NM_000426.4(LAMA2):c.2857-39T>C
Allele change: Silent

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.