Variant (rsID / SNP)
rs2108978
rs2108978 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AKAP10. Location: chromosome 17, position 19,861,458. The table records no clinical significance for this variant.
Reference-table entries
AKAP10Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:19861458
- HGVS
- NM_007202.4,c.746G>A,p.Arg249His
- Allele change
- Missense_R249H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.