RS957644 MGST3

Health Risk Chr 1:165646919 snv intron variant
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Associated Conditions
Population Frequencies
gnomAD ALL
28.7%
1kG AFR
48%
1kG ALL
77.6%
1kG AMR
15.4%
1kG EAS
97%
1kG EUR
76.2%
1kG SAS
11.6%
Other Variants in MGST3
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