RS11799886 MGST3

Health Risk Chr 1:165651554 snv intron variant
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Associated Conditions
Population Frequencies
gnomAD ALL
86.2%
1kG AFR
84.7%
1kG ALL
10.3%
1kG AMR
9.2%
1kG EAS
2.9%
1kG EUR
83.6%
1kG SAS
5.6%
Other Variants in MGST3
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