ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.21557A>G (p.Tyr7186Cys)

gnomAD frequency: 0.00001  dbSNP: rs560240166
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000733398 SCV000861464 uncertain significance not provided 2018-05-29 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000733398 SCV001153048 uncertain significance not provided 2019-04-01 criteria provided, single submitter clinical testing

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