ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.5043G>A (p.Val1681=)

dbSNP: rs1295009131
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
WangQJ Lab, Chinese People's Liberation Army General Hospital RCV001822943 SCV001762492 uncertain significance Autosomal recessive nonsyndromic hearing loss 2 2021-07-01 no assertion criteria provided clinical testing

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