Variant (rsID / SNP)
rs919364
rs919364 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DKKL1. Location: chromosome 19, position 49,867,913. The table records no clinical significance for this variant.
Reference-table entries
DKKL1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:49867913
- HGVS
- NM_014419.4,c.85G>A,p.Ala29Thr
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.