Variant (rsID / SNP)
rs906219
rs906219 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HKDC1. Location: chromosome 10, position 71,026,510. The table records no clinical significance for this variant.
Reference-table entries
HKDC1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:71026510
- HGVS
- NM_025130.4,c.2751C>A,p.Asn917Lys
- Allele change
- Missense_N917K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.