RS2214326 DNAH11

Health Risk Chr 7:21816532 snv missense variant
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Associated Conditions
Population Frequencies
gnomAD ALL
0%
1kG AFR
38.2%
1kG ALL
48.4%
1kG AMR
49.3%
1kG EAS
19.1%
1kG EUR
66.4%
1kG SAS
43.5%
Other Variants in DNAH11
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