ClinVar Miner

Submissions for variant NM_001063.4(TF):c.1765C>T (p.Pro589Ser) (rs1049296)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000376325 SCV000441233 benign Atransferrinemia 2016-06-14 criteria provided, single submitter clinical testing
OMIM RCV000013451 SCV000033698 association Transferrin variant c1/c2 2015-05-18 no assertion criteria provided literature only
OMIM RCV000013452 SCV000033699 risk factor Alzheimer disease, susceptibility to 2010-06-05 no assertion criteria provided literature only

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