Variant (rsID / SNP)
rs891512
rs891512 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOS3. Location: chromosome 7, position 150,708,089. Clinical significance in the table: Benign.
Reference-table entries
NOS3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:150708089
- Cytoband
- 7q36.1
- HGVS
- NM_000603.5(NOS3):c.2984+15A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.