Variant (rsID / SNP)
rs880633
rs880633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHI3L1. Location: chromosome 1, position 203,152,801. The table records no clinical significance for this variant.
Reference-table entries
CHI3L1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:203152801
- HGVS
- NM_001276.4,c.433A>G,p.Arg145Gly
- Allele change
- Missense_R145G
Associated conditions / phenotypes
Hepatocellular Carcinoma|Hepatitis C|Hepatitis C Virus|Hepatitis|Lung Disease|Scoliosis|Idiopathic Scoliosis|Cystic Fibrosis|Asthma|Scoliosis, Isolated 1|Pulmonary Disease, Chronic Obstructive|Cervical Cancer|Oral Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.