Variant (rsID / SNP)
rs4644
rs4644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LGALS3. Location: chromosome 14, position 55,604,935. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 14:55604935
- HGVS
- NM_001357678.2,c.233C>A,p.Pro78His
- Allele change
- Missense_P78H
Associated conditions / phenotypes
Differentiated Thyroid Carcinoma|Thyroid Carcinoma|Hyperglycemia|Rhabdomyosarcoma|Breast Cancer|Non-Alcoholic Steatohepatitis|Fatty Liver Disease, Nonalcoholic 1|Lung Cancer|Rheumatoid Arthritis|Lipoprotein Quantitative Trait Locus|Thrombophilia Due to Thrombin Defect|Arteries, Anomalies of|Atherosclerosis Susceptibility|Atrial Standstill 1|Heart Disease|Chagas Disease|Dilated Cardiomyopathy|Gastric Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.