ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.4297del (p.Gln1433fs)

dbSNP: rs1555096223
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000671977 SCV000797026 pathogenic Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2018-01-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005004347 SCV005629461 pathogenic Autosomal dominant nonsyndromic hearing loss 11; Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2024-03-05 criteria provided, single submitter clinical testing

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