Variant (rsID / SNP)
rs10746463
rs10746463 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD55. Location: chromosome 1, position 207,510,596. The table records no clinical significance for this variant.
Reference-table entries
CD55Not classified
- Variant type
- intron_variant
- Chromosome / position
- 1:207510596
- HGVS
- NM_001300902.2,c.980-78G>A
- Allele change
- Silent
Associated conditions / phenotypes
Gastric Cancer|Allergic Rhinitis|Asthma-Related Traits 4|Rhinitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.