ClinVar Miner

Submissions for variant NM_172362.3(KCNH1):c.251G>A (p.Arg84Gln)

gnomAD frequency: 0.00009  dbSNP: rs370185149
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001571640 SCV001796149 likely benign not provided 2020-04-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001571640 SCV002237466 benign not provided 2023-06-16 criteria provided, single submitter clinical testing

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