Variant (rsID / SNP)
rs2261988
rs2261988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UHRF1. Location: chromosome 19, position 4,910,889. The table records no clinical significance for this variant.
Reference-table entries
UHRF1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:4910889
- HGVS
- NM_013282.5,c.31G>T,p.Ala11Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.