Variant (rsID / SNP)
rs45582036
rs45582036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DST. Location: chromosome 6, position 56,469,319. The table records no clinical significance for this variant.
Reference-table entries
DSTNot classified
- Variant type
- missense_variant
- Chromosome / position
- 6:56469319
- HGVS
- NM_001374736.1,c.10107C>A,p.Asn3369Lys
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.