ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.3560G>T (p.Ser1187Ile)

dbSNP: rs1555090314
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000673329 SCV000798517 uncertain significance Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2018-03-19 criteria provided, single submitter clinical testing
Baylor Genetics RCV001334333 SCV001527146 uncertain significance Autosomal dominant nonsyndromic hearing loss 11 2018-12-21 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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