Variant (rsID / SNP)

rs3815550

rs3815550 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VASH1. Location: chromosome 14, position 77,236,380. The table records no clinical significance for this variant.

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Reference-table entries

VASH1Not classified

Variant type: synonymous_variant
Chromosome / position: 14:77236380
HGVS: NM_014909.5,c.384C>T,p.Tyr128Tyr
Allele change: Synonymous_Y128Y

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.