Variant (rsID / SNP)
rs699947
rs699947 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VEGFA. Location: chromosome 6, position 43,736,389. Clinical significance in the table: Benign.
Reference-table entries
VEGFABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:43736389
- Cytoband
- 6p21.1
- HGVS
- NM_001025366.2(VEGFA):c.-2055A>C
Associated conditions / phenotypes
Atherosclerosis, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.