Variant (rsID / SNP)
rs4652
rs4652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LGALS3. Location: chromosome 14, position 55,605,036. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 14:55605036
- HGVS
- NM_001357678.2,c.334A>C,p.Thr112Pro
- Allele change
- Missense_T112P
Associated conditions / phenotypes
Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Rheumatoid Arthritis|Type 2 Diabetes Mellitus|Arthritis|Cervical Cancer|Pulmonary Hypertension, Primary, 1|Scleroderma, Familial Progressive|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Systemic Scleroderma|Myopathy|Lung Cancer|Non-Alcoholic Steatohepatitis|Fatty Liver Disease, Nonalcoholic 1|Atrial Standstill 1|Heart Disease|Chagas Disease|Dilated Cardiomyopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.