ClinVar Miner

Submissions for variant NM_004700.4(KCNQ4):c.1044_1051del (p.Ala349Profs)

dbSNP: rs797044972
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000655883 SCV000777812 pathogenic Autosomal dominant nonsyndromic hearing loss 2A 2015-08-20 no assertion criteria provided literature only

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