ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.22499C>T (p.Ala7500Val)

gnomAD frequency: 0.00001  dbSNP: rs1560689342
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000732479 SCV000860444 uncertain significance not provided 2018-03-29 criteria provided, single submitter clinical testing
Revvity Omics, Revvity Omics RCV000732479 SCV003825979 uncertain significance not provided 2019-09-25 criteria provided, single submitter clinical testing

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