Variant (rsID / SNP)
rs4625783
rs4625783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC57. Location: chromosome 17, position 80,086,395. The table records no clinical significance for this variant.
Reference-table entries
CCDC57Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:80086395
- HGVS
- NM_001394669.1,c.2656A>G,p.Arg886Gly
- Allele change
- Missense_R774G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.