ClinVar Miner

Submissions for variant NM_002906.4(RDX):c.1732G>A (p.Asp578Asn)

dbSNP: rs121918379
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000014072 SCV000034319 pathogenic Autosomal recessive nonsyndromic hearing loss 24 2007-05-01 no assertion criteria provided literature only

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