ClinVar Miner

Submissions for variant NM_000844.4(GRM7):c.1026G>A (p.Thr342=)

gnomAD frequency: 0.00052  dbSNP: rs78137319
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000906359 SCV001050991 benign not provided 2025-02-11 criteria provided, single submitter clinical testing

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