Variant (rsID / SNP)
rs10016022
rs10016022 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF518B. Location: chromosome 4, position 10,446,906. The table records no clinical significance for this variant.
Reference-table entries
ZNF518BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:10446906
- HGVS
- NM_001375816.1,c.1047T>C,p.Asp349Asp
- Allele change
- Synonymous_D349D
Associated conditions / phenotypes
Gout
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.