Variant (rsID / SNP)
rs4930979
rs4930979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DENND5B. Location: chromosome 12, position 31,648,826. The table records no clinical significance for this variant.
Reference-table entries
DENND5BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 12:31648826
- HGVS
- NM_001308339.2,c.260G>A,p.Arg87Lys
- Allele change
- Missense_R52K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.