Variant (rsID / SNP)
rs2070744
rs2070744 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOS3. Location: chromosome 7, position 150,690,079. Clinical significance in the table: risk factor.
Reference-table entries
NOS3Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:150690079
- Cytoband
- 7q36.1
- HGVS
- NM_000603.5(NOS3):c.-51-762=
- Allele change
- Silent
Associated conditions / phenotypes
Coronary artery spasm 1, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.