ClinVar Miner

Submissions for variant NM_144991.3(TSPEAR):c.303+9641C>A

dbSNP: rs374354141
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001733760 SCV001984645 likely benign Autosomal recessive nonsyndromic hearing loss 98 2020-10-05 criteria provided, single submitter clinical testing

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