Variant (rsID / SNP)
rs9840317
rs9840317 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UPK1B. Location: chromosome 3, position 118,909,159. The table records no clinical significance for this variant.
Reference-table entries
UPK1BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 3:118909159
- HGVS
- NM_006952.4,c.338A>G,p.Gln113Arg
- Allele change
- Missense_Q113R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.