RS139131485 DNAAF11

Health Risk Chr 8:132572315 snv missense variant
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Associated Conditions
Population Frequencies
gnomAD ALL
99.9%
1kG AFR
100%
1kG ALL
0.1%
1kG AMR
99.9%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
0.2%
Other Variants in DNAAF11
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