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Variant (rsID / SNP)

rs298917

VWA3B

rs298917 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWA3B. Location: chromosome 2, position 98,709,684. The table records no clinical significance for this variant.

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Reference-table entries

VWA3BNot classified
Variant type
synonymous_variant
Chromosome / position
2:98709684
HGVS
NM_144992.5,c.129T>C,p.His43His
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.