Variant (rsID / SNP)
rs9664945
rs9664945 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWA2. Location: chromosome 10, position 116,008,497. The table records no clinical significance for this variant.
Reference-table entries
VWA2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:116008497
- HGVS
- NM_001272046.2,c.25G>A,p.Ala9Thr
- Allele change
- Missense_A9T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.