Variant (rsID / SNP)
rs2586776
rs2586776 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRO. Location: chromosome 18, position 48,331,524. The table records no clinical significance for this variant.
Reference-table entries
MRONot classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 18:48331524
- HGVS
- NM_001127176.3,c.471C>T,p.Asp157Asp
- Allele change
- Synonymous_D157D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.