RS73823859 UGT2B7

Drug Response Chr 4:69096382 snv intron variant
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Associated Conditions
Population Frequencies
gnomAD ALL
2.6%
1kG AFR
95.2%
1kG ALL
2.7%
1kG AMR
3.3%
1kG EAS
100%
1kG EUR
3.9%
1kG SAS
99.1%
Other Variants in UGT2B7
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