Variant (rsID / SNP)
rs220109
rs220109 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UMODL1. Location: chromosome 21, position 43,522,349. The table records no clinical significance for this variant.
Reference-table entries
UMODL1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:43522349
- HGVS
- NM_173568.4,c.1260T>C,p.Ser420Ser
- Allele change
- Synonymous_S348S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.