ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.504+66A>C

gnomAD frequency: 0.02083  dbSNP: rs62638203
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000086057 SCV001787716 likely benign not provided 2019-08-04 criteria provided, single submitter clinical testing
Retina International RCV000086057 SCV000118201 not provided not provided no assertion provided not provided

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