ClinVar Miner

Submissions for variant NM_152657.4(GGN):c.1104G>A (p.Gly368=)

gnomAD frequency: 0.00073  dbSNP: rs148446446
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000955037 SCV001101715 benign not provided 2018-06-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000955037 SCV004141572 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing GGN: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000955037 SCV005308563 benign not provided criteria provided, single submitter not provided

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