RS35865357 DNAH11

Health Risk Chr 7:21765476 snv missense variant
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Associated Conditions
Population Frequencies
gnomAD ALL
98.3%
1kG AFR
99.8%
1kG ALL
99.4%
1kG AMR
1.2%
1kG EAS
100%
1kG EUR
1%
1kG SAS
0.9%
Other Variants in DNAH11
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