Variant (rsID / SNP)
rs2070371
rs2070371 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HUNK. Location: chromosome 21, position 33,368,188. The table records no clinical significance for this variant.
Reference-table entries
HUNKNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:33368188
- HGVS
- NM_014586.2,c.1413T>C,p.Leu471Leu
- Allele change
- Synonymous_L471L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.