ClinVar Miner

Submissions for variant NM_001143831.3(GRM5):c.1394+8_1394+9del

dbSNP: rs376748672
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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
Labcorp Genetics (formerly Invitae), Labcorp RCV000891716 SCV001035543 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000891716 SCV004131258 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing GRM5: BP4, BS2

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