Variant (rsID / SNP)
rs7980045
rs7980045 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWF. Location: chromosome 12, position 6,204,615. Clinical significance in the table: Benign.
Reference-table entries
VWFBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:6204615
- Cytoband
- 12p13.31
- HGVS
- NM_000552.5(VWF):c.657+11A>C
- Allele change
- Silent
Associated conditions / phenotypes
von Willebrand disorder|von Willebrand disease type 1|von Willebrand disease type 3|von Willebrand disease type 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.