ClinVar Miner

Submissions for variant NM_000844.4(GRM7):c.114C>T (p.Tyr38=)

gnomAD frequency: 0.00063  dbSNP: rs114869468
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV000956067 SCV005245656 benign not provided criteria provided, single submitter not provided
Labcorp Genetics (formerly Invitae), Labcorp RCV000956067 SCV001102810 benign not provided 2026-01-27 criteria provided, single submitter clinical testing

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