ClinVar Miner

Submissions for variant NM_144991.3(TSPEAR):c.304-5450G>T

dbSNP: rs143105755
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001335434 SCV001528584 uncertain significance Autosomal recessive nonsyndromic hearing loss 98 2018-05-08 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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