Variant (rsID / SNP)
rs4955418
rs4955418 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC71. Location: chromosome 3, position 49,200,627. The table records no clinical significance for this variant.
Reference-table entries
CCDC71Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:49200627
- HGVS
- NM_022903.4,c.1015T>C,p.Trp339Arg
- Allele change
- Missense_W339R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.