Variant (rsID / SNP)
rs4359426
rs4359426 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCL22. Location: chromosome 16, position 57,392,733. The table records no clinical significance for this variant.
Reference-table entries
CCL22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:57392733
- HGVS
- NM_002990.5,c.5A>C,p.Asp2Ala
- Allele change
- Missense_D2A
Associated conditions / phenotypes
Myocardial Infarction|Dermatitis|Human Immunodeficiency Virus Type 1|Dermatitis, Atopic|Skin Disease|Heart Disease|Breast Cancer|Intermediate Coronary Syndrome|Colorectal Adenocarcinoma|Adenocarcinoma|Cytokine Deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.