RS1801265 DPYD

Health Risk Chr 1:97883328 snv missense variant
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What This Variant Does
"Technology to accelerate pangenomic scanning for unknown point mutations in exonic sequences: cyclin...
Associated Conditions
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Body mass index G β: 0.013 2E-16 PubMed
Body mass index G β: 0.013 9E-10 PubMed
Population Frequencies
gnomAD ALL
77.9%
1kG AFR
44.2%
1kG ALL
26%
1kG AMR
22.5%
1kG EAS
91.4%
1kG EUR
78.5%
1kG SAS
26.6%
Other Variants in DPYD
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