Variant (rsID / SNP)
rs11063962
rs11063962 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWF. Location: chromosome 12, position 6,076,781. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
VWFBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:6076781
- Cytoband
- 12p13.31
- HGVS
- NM_000552.5(VWF):c.7771-13C>T
- Allele change
- Silent
Associated conditions / phenotypes
von Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 3|von Willebrand disease type 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.