Variant (rsID / SNP)
rs2305398
rs2305398 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAND2. Location: chromosome 3, position 12,856,856. The table records no clinical significance for this variant.
Reference-table entries
CAND2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:12856856
- HGVS
- NM_001162499.2,c.1223A>G,p.Gln408Arg
- Allele change
- Missense_Q408R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.