ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.21829A>G (p.Asn7277Asp)

gnomAD frequency: 0.00003  dbSNP: rs758247611
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) RCV000282700 SCV000334502 uncertain significance not provided 2015-08-18 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000282700 SCV003822134 uncertain significance not provided 2020-03-30 criteria provided, single submitter clinical testing

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