Variant (rsID / SNP)
rs2231524
rs2231524 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRAC1. Location: chromosome 8, position 141,525,327. The table records no clinical significance for this variant.
Reference-table entries
CHRAC1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 8:141525327
- HGVS
- NM_017444.6,c.377A>G,p.His126Arg
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.