ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.26008C>G (p.Pro8670Ala)

dbSNP: rs1577904664
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000997525 SCV001153026 uncertain significance not provided 2019-05-01 criteria provided, single submitter clinical testing

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