Variant (rsID / SNP)
rs544864
rs544864 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPEG1. Location: chromosome 11, position 58,978,940. The table records no clinical significance for this variant.
Reference-table entries
MPEG1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:58978940
- HGVS
- NM_001039396.2,c.1399G>A,p.Ala467Thr
- Allele change
- Missense_A467T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.