ClinVar Miner

Submissions for variant NM_017662.5(TRPM6):c.2239-10dup

dbSNP: rs771018979
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
Labcorp Genetics (formerly Invitae), Labcorp RCV003717248 SCV004510965 benign not provided 2023-12-28 criteria provided, single submitter clinical testing

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