Variant (rsID / SNP)
rs13180
rs13180 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IREB2. Location: chromosome 15, position 78,789,488. The table records no clinical significance for this variant.
Reference-table entries
IREB2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 15:78789488
- HGVS
- NM_004136.4,c.2616C>T,p.Ala872Ala
- Allele change
- Synonymous_A815A
Associated conditions / phenotypes
Pulmonary Disease, Chronic Obstructive|Alzheimer Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.