ClinVar Miner

Submissions for variant NM_005915.6(MCM6):c.2428T>C (p.Tyr810His)

gnomAD frequency: 0.00036  dbSNP: rs55660827
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pathology and Clinical Laboratory Medicine, King Fahad Medical City RCV001261629 SCV001438922 benign not specified criteria provided, single submitter clinical testing
OMIM RCV001822870 SCV000028334 pathogenic Lactase persistence 2008-01-01 no assertion criteria provided literature only

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