Variant (rsID / SNP)
rs2427285
rs2427285 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA5. Location: chromosome 20, position 60,900,579. The table records no clinical significance for this variant.
Reference-table entries
LAMA5Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:60900579
- HGVS
- NM_005560.6,c.5322G>T,p.Thr1774Thr
- Allele change
- Synonymous_T1774T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.