ClinVar Miner

Submissions for variant NM_003307.4(TRPM2):c.1923C>G (p.Ile641Met)

gnomAD frequency: 0.00150  dbSNP: rs150484698
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000885572 SCV001029029 likely benign not provided 2018-07-11 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000885572 SCV004146655 benign not provided 2022-07-01 criteria provided, single submitter clinical testing TRPM2: BS1, BS2

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