Variant (rsID / SNP)
rs9554897
rs9554897 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC168. Location: chromosome 13, position 103,383,417. The table records no clinical significance for this variant.
Reference-table entries
CCDC168Not classified
- Variant type
- missense_variant
- Chromosome / position
- 13:103383417
- HGVS
- NM_001146197.3,c.19630A>G,p.Lys6544Glu
- Allele change
- Missense_K6544E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.