RS117350233 ATP2A1

Health Risk Chr 16:28894526 snv missense variant
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Associated Conditions
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
99.7%
1kG EUR
100%
1kG SAS
100%
Other Variants in ATP2A1
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