Variant (rsID / SNP)
rs55687637
rs55687637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWF. Location: chromosome 12, position 6,076,640. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
VWFConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:6076640
- Cytoband
- 12p13.31
- HGVS
- NM_000552.5(VWF):c.7887+12T>C
- Allele change
- Silent
Associated conditions / phenotypes
von Willebrand disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.