Variant (rsID / SNP)

rs27434

rs27434 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERAP1. Location: chromosome 5, position 96,129,512. The table records no clinical significance for this variant.

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Reference-table entries

ERAP1Not classified

Variant type: synonymous_variant
Chromosome / position: 5:96129512
HGVS: NM_001349244.2,c.1068T>C,p.Ala356Ala
Allele change: Synonymous_A356A

Associated conditions / phenotypes

Inflammatory Spondylopathy|Spondyloarthropathy 1|Spondylitis|Uveitis|Iridocyclitis

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.