Variant (rsID / SNP)
rs2230804
rs2230804 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHUK. Location: chromosome 10, position 101,977,883. The table records no clinical significance for this variant.
Reference-table entries
CHUKNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:101977883
- HGVS
- NM_001278.5,c.802G>A,p.Val268Ile
- Allele change
- Missense_V268I
Associated conditions / phenotypes
Stroke, Ischemic|Ige Responsiveness, Atopic
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.