Variant (rsID / SNP)
rs944895
rs944895 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA5. Location: chromosome 20, position 60,887,581. The table records no clinical significance for this variant.
Reference-table entries
LAMA5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 20:60887581
- HGVS
- NM_005560.6,c.9235C>T,p.Arg3079Trp
- Allele change
- Missense_R3079W
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.