Variant (rsID / SNP)
rs662471
rs662471 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA1. Location: chromosome 18, position 7,008,591. The table records no clinical significance for this variant.
Reference-table entries
LAMA1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:7008591
- HGVS
- NM_005559.4,c.4018A>G,p.Met1340Val
- Allele change
- Missense_M1340V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.