ClinVar Miner

Submissions for variant NM_004442.7(EPHB2):c.835G>T (p.Ala279Ser) (rs35882952)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000894397 SCV001038378 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
OMIM RCV000009059 SCV000029276 pathogenic Prostate cancer/brain cancer susceptibility 2004-09-01 no assertion criteria provided literature only

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