Variant (rsID / SNP)
rs7968231
rs7968231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP54. Location: chromosome 12, position 97,102,578. The table records no clinical significance for this variant.
Reference-table entries
CFAP54Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:97102578
- HGVS
- NM_001367885.1,c.6916G>A,p.Glu2306Lys
- Allele change
- Missense_E2241K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.