Variant (rsID / SNP)
rs1786263
rs1786263 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP192. Location: chromosome 18, position 13,116,432. The table records no clinical significance for this variant.
Reference-table entries
CEP192Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:13116432
- HGVS
- NM_032142.4,c.7346G>T,p.Arg2449Leu
- Allele change
- Missense_R2449L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.