ClinVar Miner

Submissions for variant NM_017636.4(TRPM4):c.2674C>T (p.Arg892Cys) (rs147854826)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000330330 SCV000414305 uncertain significance Progressive familial heart block 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000858445 SCV000549930 benign not provided 2018-10-01 criteria provided, single submitter clinical testing
Division of Human Genetics,Children's Hospital of Philadelphia RCV000469849 SCV000536899 uncertain significance Progressive familial heart block type 1B 2016-07-19 no assertion criteria provided research

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