ClinVar Miner

Submissions for variant NM_001375978.1(CHRM3):c.328C>T (p.Leu110=)

gnomAD frequency: 0.00037  dbSNP: rs111407169
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 RCV000894535 SCV001038523 likely benign not provided 2023-01-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501493 SCV002807644 likely benign Prune belly syndrome 2021-10-05 criteria provided, single submitter clinical testing

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