Variant (rsID / SNP)

rs3213809

rs3213809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERAP1. Location: chromosome 5, position 96,127,833. The table records no clinical significance for this variant.

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Reference-table entries

ERAP1Not classified

Variant type: synonymous_variant
Chromosome / position: 5:96127833
HGVS: NM_001349244.2,c.1251C>T,p.His417His
Allele change: Synonymous_H417H

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.