ClinVar Miner

Submissions for variant NM_012463.4(ATP6V0A2):c.548G>A (p.Gly183Glu)

dbSNP: rs1555296748
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000504303 SCV000593526 uncertain significance not specified 2015-12-03 criteria provided, single submitter clinical testing

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