RS137882374 GH1

Health Risk Chr 17:63917852 snv missense variant
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Associated Conditions
Population Frequencies
gnomAD ALL
0%
1kG AFR
98.9%
1kG ALL
0.3%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in GH1
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