ClinVar Miner

Submissions for variant NM_000544.3(TAP2):c.2059C>T (p.Gln687Ter) (rs241448)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000545577 SCV000642019 benign Bare lymphocyte syndrome type 1 2017-11-22 criteria provided, single submitter clinical testing
OMIM RCV000014729 SCV000034984 benign PEPTIDE TRANSPORTER PSF2 POLYMORPHISM 1992-05-01 no assertion criteria provided literature only

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