Variant (rsID / SNP)
rs2250982
rs2250982 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UHRF1. Location: chromosome 19, position 4,945,914. The table records no clinical significance for this variant.
Reference-table entries
UHRF1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:4945914
- HGVS
- NM_013282.5,c.1386A>C,p.Ile462Ile
- Allele change
- Synonymous_I449I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.