Variant (rsID / SNP)

rs3810818

rs3810818 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VASN, CORO7. Location: chromosome 16, position 4,432,029. The table records no clinical significance for this variant.

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Reference-table entries

VASNNot classified

Variant type: missense_variant
Chromosome / position: 16:4432029
HGVS: NM_138440.3,c.1151A>C,p.Glu384Ala
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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