Variant (rsID / SNP)
rs6062223
rs6062223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA5. Location: chromosome 20, position 60,909,316. The table records no clinical significance for this variant.
Reference-table entries
LAMA5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 20:60909316
- HGVS
- NM_005560.6,c.2665G>A,p.Val889Met
- Allele change
- Missense_V889M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.