RS3788853 XPNPEP2

Health Risk Chr X:129736813 snv intergenic variant

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What This Variant Does

"A form of this snp, located upstream of the XPNPEP2 gene on the X chromosome, may cause susceptibili...

Associated Conditions

Susceptibility to angioedema induced by ACE inhibitors

GWAS Studies (1)

Trait	Risk Allele	OR / Beta	P-value	Study
Serum uric acid levels	A	β: 0.009	4E-8	PubMed

ClinVar Assertions (2)

NC_000023.11:g.129736814C>A

· 1 submitter

NC_000023.11:g.129736814C>A

· 1 submitter

Population Frequencies

1kG AFR

25.6%

1kG ALL

23.1%

1kG AMR

77.5%

1kG EAS

74.7%

1kG EUR

79%

1kG SAS

80.1%