ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.6459del (p.Phe2154fs)

dbSNP: rs1555111077
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000668360 SCV000792944 uncertain significance Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2017-08-02 criteria provided, single submitter clinical testing

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