Variant (rsID / SNP)
rs2303759
rs2303759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DKKL1. Location: chromosome 19, position 49,869,051. The table records no clinical significance for this variant.
Reference-table entries
DKKL1Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 19:49869051
- HGVS
- NM_014419.4,c.326T>G,p.Met109Arg
- Allele change
- Missense_M34R
Associated conditions / phenotypes
Multiple Sclerosis|Pediatric Multiple Sclerosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.