ClinVar Miner

Submissions for variant NM_001201543.2(FAM161A):c.1584-11G>A

gnomAD frequency: 0.17214  dbSNP: rs17513666
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000667588 SCV000792065 benign Retinitis pigmentosa 28 2017-06-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001513056 SCV001720589 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000667588 SCV001761868 benign Retinitis pigmentosa 28 2021-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001513056 SCV005244275 benign not provided criteria provided, single submitter not provided

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