Variant (rsID / SNP)
rs474337
rs474337 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP192. Location: chromosome 18, position 13,095,609. The table records no clinical significance for this variant.
Reference-table entries
CEP192Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:13095609
- HGVS
- NM_032142.4,c.6362T>C,p.Leu2121Pro
- Allele change
- Missense_L2121P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.