Variant (rsID / SNP)
rs2231495
rs2231495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADA2. Location: chromosome 22, position 17,669,306. The table records no clinical significance for this variant.
Reference-table entries
ADA2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 22:17669306
- HGVS
- NM_001282225.2,c.1004A>G,p.His335Arg
- Allele change
- Missense_H293R
Associated conditions / phenotypes
Missense_H293R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.