ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.276G>A (p.Glu92=)

gnomAD frequency: 0.00005  dbSNP: rs1407023193
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000788138 SCV000927156 uncertain significance not provided 2017-02-16 criteria provided, single submitter clinical testing

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