Variant (rsID / SNP)
rs1800684
rs1800684 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGER. Location: chromosome 6, position 32,151,994. The table records no clinical significance for this variant.
Reference-table entries
AGERNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:32151994
- HGVS
- NM_001206929.2,c.6T>A,p.Ala2Ala
- Allele change
- Synonymous_A2A
Associated conditions / phenotypes
Colorectal Cancer|Rectum Cancer|Synonymous_A2A|Synonymous_A2A|Synonymous_A2A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.