Variant (rsID / SNP)
rs10798674
rs10798674 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AXDND1. Location: chromosome 1, position 179,347,832. The table records no clinical significance for this variant.
Reference-table entries
AXDND1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:179347832
- HGVS
- NM_144696.6,c.435T>C,p.Val145Val
- Allele change
- Synonymous_V145V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
