ClinVar Miner

Submissions for variant NM_153700.2(STRC):c.4765G>T (p.Val1589Phe)

dbSNP: rs147963245
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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 RCV001822953 SCV001762503 uncertain significance Autosomal recessive nonsyndromic hearing loss 16 2021-07-01 no assertion criteria provided clinical testing

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