ClinVar Miner

Submissions for variant NM_001038603.3(MARVELD2):c.1208_1211del (p.Arg403fs)

dbSNP: rs772030670
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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 RCV001822914 SCV001762443 likely pathogenic Autosomal recessive nonsyndromic hearing loss 49 2021-07-01 no assertion criteria provided clinical testing

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