ClinVar Miner

Submissions for variant NM_001252024.2(TRPM1):c.4-36G>A

gnomAD frequency: 0.85121  dbSNP: rs4779817
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001608913 SCV001833357 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838698 SCV002098834 benign Congenital stationary night blindness 1C 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001608913 SCV005293493 benign not provided criteria provided, single submitter not provided

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