Variant (rsID / SNP)
rs148582730
rs148582730 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CILP. Location: chromosome 15, position 65,490,592. The table records no clinical significance for this variant.
Reference-table entries
CILPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 15:65490592
- HGVS
- NM_003613.4,c.2032G>A,p.Val678Met
- Allele change
- Missense_V678M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.