ClinVar Miner

Submissions for variant NM_000363.5(TNNI3):c.550-10C>T (rs201240150)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000036304 SCV000059956 likely benign not specified 2015-11-24 criteria provided, single submitter clinical testing c.550-10C>T in intron 7 of TNNI3: This variant is not expected to have clinical significance because it has been identified in 0.6% (61/9712) of African chromos omes by the Exome Aggregation Consortium (ExAC, http://exac.broadinstitute.org; dbSNP rs201240150).
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000036304 SCV000232536 benign not specified 2015-04-24 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000036304 SCV000303837 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000472754 SCV000562163 benign Hypertrophic cardiomyopathy 2020-12-02 criteria provided, single submitter clinical testing
Color Health, Inc RCV000777814 SCV000913809 benign Cardiomyopathy 2018-06-18 criteria provided, single submitter clinical testing

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