Variant (rsID / SNP)
rs25648
rs25648 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VEGFA. Location: chromosome 6, position 43,738,977. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- synonymous_variant
- Chromosome / position
- 6:43738977
- HGVS
- NM_001025366.3,c.534C>T,p.Ser178Ser
- Allele change
- Synonymous_S178S
Associated conditions / phenotypes
Bladder Cancer|Pre-Eclampsia|Gastric Cancer|Eclampsia|Cervical Cancer|Goiter|Nodular Goiter|Thyroid Cancer, Nonmedullary, 1|Colorectal Cancer|Thyroid Carcinoma|Neutropenia|Kawasaki Disease|Hepatocellular Carcinoma|Rheumatoid Arthritis|Leukemia, Chronic Lymphocytic|Pseudoxanthoma Elasticum|Microvascular Complications of Diabetes 5|Microvascular Complications of Diabetes 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.