Variant (rsID / SNP)
rs3813089
rs3813089 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRO. Location: chromosome 18, position 48,346,024. The table records no clinical significance for this variant.
Reference-table entries
MRONot classified
- Variant type
- missense_variant
- Chromosome / position
- 18:48346024
- HGVS
- NM_001127176.3,c.68C>A,p.Thr23Asn
- Allele change
- Missense_T23N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.