ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.2437-6G>A

gnomAD frequency: 0.03215  dbSNP: rs114970739
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
Invitae RCV000086052 SCV001723559 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000086052 SCV001895807 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Retina International RCV000086052 SCV000118196 not provided not provided no assertion provided not provided

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