RS139515054 XDH

Health Risk Chr 2:31341377 snv missense variant

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Associated Conditions

Xanthinuria type II

Hereditary xanthinuria type 1

XDH-related disorder

Xanthinuria type II

Hereditary xanthinuria type 1

XDH-related disorder

GWAS Studies (1)

Trait	Risk Allele	OR / Beta	P-value	Study
Urate levels	G	OR: 0.11	3E-9	PubMed

Population Frequencies

gnomAD ALL

0.3%

1kG AFR

100%

1kG ALL

100%

1kG AMR

100%

1kG EAS

100%

1kG EUR

0.2%

1kG SAS

100%

Other Variants in XDH