Variant (rsID / SNP)
rs4808551
rs4808551 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPAMD8. Location: chromosome 19, position 17,111,297. The table records no clinical significance for this variant.
Reference-table entries
CPAMD8Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:17111297
- HGVS
- NM_015692.5,c.794T>C,p.Met265Thr
- Allele change
- Missense_M312T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.