ClinVar Miner

Submissions for variant NM_005422.4(TECTA):c.5586+40C>G

dbSNP: rs2186747
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001687045 SCV001901352 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838784 SCV002098514 benign Autosomal dominant nonsyndromic hearing loss 12 2021-09-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838785 SCV002098525 benign Autosomal recessive nonsyndromic hearing loss 21 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001687045 SCV005235296 benign not provided criteria provided, single submitter not provided

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