ClinVar Miner

Submissions for variant NM_024334.3(TMEM43):c.982C>A (p.Arg328=)

dbSNP: rs561883271
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
Color Diagnostics, LLC DBA Color Health RCV001178036 SCV001342364 likely benign Cardiomyopathy 2019-10-30 criteria provided, single submitter clinical testing

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