ClinVar Miner

Submissions for variant NM_000843.4(GRM6):c.1500+23A>G

gnomAD frequency: 0.57932  dbSNP: rs2256966
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001701598 SCV001934000 benign Congenital stationary night blindness 1B 2021-08-10 criteria provided, single submitter clinical testing
GeneDx RCV000086027 SCV001950616 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Retina International RCV000086027 SCV000118170 not provided not provided no assertion provided not provided

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