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Variant (rsID / SNP)

rs2276053

VWA5A

rs2276053 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VWA5A. Location: chromosome 11, position 124,006,993. The table records no clinical significance for this variant.

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Reference-table entries

VWA5ANot classified
Variant type
missense_variant
Chromosome / position
11:124006993
HGVS
NM_001130142.2,c.1517G>A,p.Arg506Lys
Allele change
Missense_R506K

Public references

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