RS1368408 SCGB3A2

Health Risk Chr 5:147878598 snv intron variant
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Associated Conditions
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
SCGB3A2 protein levels A OR: 0.13 1E-61 PubMed
Population Frequencies
gnomAD ALL
15.9%
1kG AFR
66%
1kG ALL
76.2%
1kG AMR
66.4%
1kG EAS
21.5%
1kG EUR
14.2%
1kG SAS
84.9%
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