ClinVar Miner

Submissions for variant NM_182548.4(LHFPL5):c.*477TA[3]

dbSNP: rs879430131
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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 RCV004577870 SCV000462769 uncertain significance Hearing loss, autosomal recessive 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695931 SCV005188920 uncertain significance not provided criteria provided, single submitter not provided

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