RS3752988 CYP2C8

Health Risk Chr 10:95065125 snv intron variant
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Associated Conditions
Population Frequencies
1kG AFR
48.9%
1kG ALL
39.7%
1kG AMR
29%
1kG EAS
61.9%
1kG EUR
64.4%
1kG SAS
40.8%
Other Variants in CYP2C8
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