Variant (rsID / SNP)
rs597371
rs597371 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWA2. Location: chromosome 10, position 116,032,519. The table records no clinical significance for this variant.
Reference-table entries
VWA2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:116032519
- HGVS
- NM_001272046.2,c.392A>G,p.Glu131Gly
- Allele change
- Missense_E131G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.