RS9332220 CYP2C9

Health Risk Chr 10:94984185 snv intron variant
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Associated Conditions
Population Frequencies
1kG AFR
21%
1kG ALL
83.6%
1kG AMR
84.9%
1kG EAS
91.2%
1kG EUR
80.2%
1kG SAS
15.5%
Other Variants in CYP2C9
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