ClinVar Miner

Submissions for variant NM_000601.6(HGF):c.88+9C>T

gnomAD frequency: 0.00001  dbSNP: rs199638850
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000321516 SCV000470120 uncertain significance Nonsyndromic Hearing Loss, Mixed 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005090590 SCV005803109 likely benign not provided 2024-10-30 criteria provided, single submitter clinical testing

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