Variant (rsID / SNP)
rs3783185
rs3783185 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLYBL. Location: chromosome 13, position 100,518,580. The table records no clinical significance for this variant.
Reference-table entries
CLYBLNot classified
- Variant type
- missense_variant
- Chromosome / position
- 13:100518580
- HGVS
- NM_001393356.1,c.721A>G,p.Ile241Val
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.