Variant (rsID / SNP)

rs34261036

rs34261036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERAP2, ERAP1. Location: chromosome 5, position 96,231,056. Clinical significance in the table: Benign.

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Reference-table entries

ERAP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:96231056
Cytoband: 5q15
HGVS: NM_022350.5(ERAP2):c.1232T>G (p.Leu411Arg)
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.