RS137955120 AP2A1

Health Risk Chr 19:49807196 snv missense variant
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Associated Conditions
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
0.2%
1kG SAS
100%
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