Variant (rsID / SNP)
rs11218891
rs11218891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JHY. Location: chromosome 11, position 122,795,688. The table records no clinical significance for this variant.
Reference-table entries
JHYNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:122795688
- HGVS
- NM_001363089.2,c.948T>C,p.Asp316Asp
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.