Variant (rsID / SNP)

rs3788853

rs3788853 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XPNPEP2. Clinical significance in the table: risk factor.

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Reference-table entries

XPNPEP2Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Cytoband: Xq26.1
HGVS: NG_011479.1:g.2846C>A

Associated conditions / phenotypes

Susceptibility to angioedema induced by ACE inhibitors

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.