Variant (rsID / SNP)

rs1056893

rs1056893 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERAP2, ERAP1. Location: chromosome 5, position 96,245,439. The table records no clinical significance for this variant.

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Reference-table entries

ERAP2Not classified

Variant type: synonymous_variant
Chromosome / position: 5:96245439
HGVS: NM_001130140.2,c.2325C>T,p.Ser775Ser
Allele change: Silent

Associated conditions / phenotypes

Mycobacterium Tuberculosis 1

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.