ClinVar Miner

Submissions for variant NM_000041.4(APOE):c.43+520G>A

gnomAD frequency: 0.39475  dbSNP: rs769450
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pharmacogenomics Lab, Chungbuk National University RCV000845579 SCV000889944 drug response Warfarin response 2010-08-31 no assertion criteria provided research

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